Nucleic acid sequences encoding protein allergens of the species Cynodon dactylon

ABSTRACT

The present invention provides nucleic acid sequences coding Cyn dI, or at least one fragment thereof or the functional equivalent of such nucleic acid sequences. The present invention also provides expression vectors comprising such nucleic acid sequences and host cells transformed therewith. The present invention further provides isolated Bermuda grass pollen protein allergen Cyn dI or fragments thereof. Isolated Bermuda grass pollen protein allergens or antigenic or allergenic fragments thereof are useful for diagnosing and treating sensitivity in an individual to Bermuda grass pollen allergens.

BACKGROUND OF THE INVENTION

Bermuda grass (Cynodon dactylon) is an important source of pollen allergens in many areas of the world, especially in tropical and sub-tropical climates. These allergens have been studied by a number of means including IgE immunoblotting (Ford D., and Baldo, B. A. J. Allergy Clin. Immunol. 79: 711-720 (1987); Shen H. D., et al., Clin. Allergy 18: 401-409 (1988), column chromatography (Orren, A., and Dowdle, S. Afr. Med. J. 51: 586 (1977); Matthiesen et al., J. Allergy Clin. Immunol. 81: 266 (Ab) (1988)), and immunoelectrophoresis (Matthiesen et al., supra, 1988).

The major allergen of Bermuda grass pollen allergen has been identified as a protein with a molecular weight (MW) in the range of 30-34 kD, binding IgE from sera of more than 76% of individuals allergic to Bermuda grass (Ford and Baldo, (1987) Supra; Shen et al, (1988) Supra, and has been designated Cyn dI (Kahn and Marsh, (1986) Mol. Immunol., 23:1281-1288; Marsh et al., (1988) Ann. Allergy, 60:499-504, Matthiesen et al, 1988, Supra). Cyn dI is a member of the Group I family of allergens (Kahn and Marsh, (1986) Supra, found in many taxonomically related grasses including ryegrass (Lol pI), Kentucky bluegrass (Poa pI) and Timothy grass (Phl pI) (Standring et al, 1987 Int. Archs Allergy Appl. Immun., 83, 96-103; Esch and Klapper, (1987) J. Allergy Clin. Immunol., 79:489-495; Matthiesen and Lowenstein (1991) Clin. Exp. Allergy,21, 309-320. However, the allergens of Bermuda grass show limited antibody cross-reactivity with those of other grasses (March et al., Supra, Berstein et al. (1976) J. Allergy Clin. Immunol.,57:141-152. A number of studies have shown that Cyn dI differs from the Group I homologues of closely related grasses (Matthiesen and Lowenstein, (1991) Supra. The sequence of the first 27 amino acids at the N-terminus of Cyn dI has been determined. (Matthiesen et al, 1988, Supra; Matthiesen et al, (1990) Epitopes of Atopic Allergens, Brussels, UCB Institute of Allergy, 9-13; Singh et al, Monographs in Allergy, (1990), 28:101-120; Matthiesen and Lowenstein, (1991), supra).

The presence of Bermuda grass pollen allergens in the environment causes hayfever and seasonal asthma in many individuals and continues to have significant socio-economic impact on Western communities. While the available spectrum of drugs, including anti-histamines and steroids, have resulted in improvement in the treatment of allergic disease, they do have unfortunate side-effects associated with long term usage. Because of these problems, renewed interest has been shown in the immunotherapy of allergic disease. Immunotherapy involves the injection of potent allergen extracts to desensitize patients against allergic reactions (Bousquet, J. and Michel, F. B., (1989) Allergy and Clin Immol. News 1: 7-10. Unfortunately, the pollen preparations used as allergens are polyvalent and of poor quality. Consequently, crude extracts are frequently used at high concentrations and may trigger potentially lethal systemic reactions, including anaphylaxis. The product expressed from the cloned gene, fragments thereof, or synthetic peptides based on the sequence of the allergens provide a safer medium for therapy since they can be quality controlled, characterized and standardized, and they optimally do not bind IgE.

SUMMARY OF THE INVENTION

The present invention provides nucleic acid sequences coding for the major protein allergen of the species Cynodon dacrylon (Cyn dI), or at least one fragment thereof or the functional equivalent of such nucleic acid sequences. The present invention also provides expression vectors comprising such nucleic acid sequences and host cells transformed therewith. The present invention further provides isolated recombinantly, chemically or synthetically produced Cyn dI or fragments thereof. Isolated Cyn dI or antigenic fragments thereof are useful for diagnosing and treating sensitivity in an individual to Bermuda grass pollen allergens.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows the nucleotide sequence (SEQ ID NO: 1) coding for and deduced partial amino acid sequence (SEQ ID NO: 2) of Cyn dI derived from a cDNA clone designated clone 2 (C2).

FIG. 2 shows a partial nucleotide sequence (SEQ ID NO: 3) coding for and deduced partial amino acid sequence (SEQ ID NO: 4) of Cyn dI, derived from a cDNA clone designated clone 18 (C18).

FIG. 3 shows a comparison of the nucleic acid sequences of clones 2 (SEQ ID NO: 1) and 18.

FIG. 4 shows a comparison of the deduced amino acid sequences of clones 2 (SEQ ID NO: 3) and 18 (SEQ ID NO: 3).

FIG. 5 shows a comparison of the deduced amino acid sequences of 7 clones coding for Cyn dI; clone 18 (SEQ ID NO:4), (C18) (SEQ ID NO:4), clone 22 (C22) (SEQ ID NO:5), clone 23 (C23) (SEQ ID NO: 5) clone 2 (C2) (SEQ ID NO: 2), clone 3 (C3) (SEQ ID NO: 7), clone 21 (C21) (SEQ ID NO: 8), and clone 33 (C33) (SEQ ID NO: 9);

FIG. 6 shows a partial nucleotide sequence (SEQ ID NO: 10) coding for and deduced partial amino acid sequence (SEQ ID NO: 11) of Cyn dI derived from a cDNA clone designated clone 14a1.

FIG. 7 shows the partial nucleotide sequence (SEQ ID NO: 12) coding for partial and deduced partial amino acid sequence (SEQ ID NO: 13) of Cyn dI derived from a cDNA clone designated clone 14c1.

FIG. 8 shows a partial amino acid sequence (SEQ ID NO: 13) of Cyn dI designated Cyn dI.14 predicted from a composite of clones 14a1 and 14c 1.

FIG. 9 shows a predicted full-length amino acid sequence (SEQ ID NO: 15) of Cyn dI designated Cyn dI.18.

FIG. 10 shows a predicted partial amino acid sequence (SEQ ID NO: 15) of Cyn dI designated Cyn dI.2/3.

FIG. 11a shows separation by SDS-PAGE of protein fractions obtained by the primary preparative isoelectric focusing (IEF) of these proteins on the Rotofor.

FIG. 11b shows a Western blot of separated proteins screened with MAb3.2.

FIG. 12a shows a separation by SDS-PAGE of protein fractions obtained by refractionation on the Rotofor of pooled fractions, 10-13, from a primary separation of crude pollen extract.

FIG. 12b shows separation by SDS-PAGE of protein fractions obtained by refractionation on the Rotofor of pooled fractions, 15-20, from a primary separation of crude pollen extract.

FIG. 13 shows Western blots of native Cyn dIa and Cyn dIb separated by SDS-PAGE and probed with IgE from sera of individuals allergic to Bermuda grass.

FIG. 14 shows binding of MAbs 1D1, 3A2, 3C2 and 4D2 to cDNA clones from a Cyn dI λgtII library. The number on the overlay corresponds to the cDNA clone number.

FIG. 15 shows a partial nucleotide sequence (SEQ ID NO: 17) coding for and deduced partial amino acid sequence (SEQ ID NO: 7) of Cyn dI derived from a CDNA clone designated clone 3.

FIG. 16 shows a partial nucleotide sequence (SEQ ID NO: 18) coding for and deduced partial amino acid (SEQ ID NO: 7) sequence (SEQ ID NO: 5) of Cyn dI derived from a cDNA clone designated clone 22.

FIG. 17 shows a partial nucleotide sequence (SEQ ID NO: 19) coding for and deduced partial amino acid (SEQ ID NO: 5) sequence of Cyn dI derived from a cDNA clone designated clone 23.

FIG. 18 shows a nucleotide sequence (SEQ ID NO: 20) and deduced amino acid sequence (SEQ ID NO: 21) of Cyn dI derived from a full-length cDNA clone designated CD1.

FIG. 19 shows a partial nucleotide (SEQ ID NO: 22) and deduced amino acid (SEQ ID NO: 5) sequence (SEQ ID NO: 23) of Cyn dI derived from a cDNA clone designated KAT-39-1.

FIG. 20 shows the comparison of predicted full-length amino acid sequences (SEQ ID NO: 23) of the Cyn dI mature proteins designated Cyn dI.18 (SEQ ID NO: 15), Cyn dI.CD1 (SEQ ID NO: 21) and Cyn dI.2/3 (full-length) (SEQ ID NO: 24).

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides nucleic acid sequences, or the functional equivalents thereof, coding for Cyn dI, the major allergen found in Bermuda grass pollen. Cyn dI appears to be a family of closely related allergens. As defined herein, a “family of allergens” are proteins related in function and amino acid sequence but encoded by genes at separate genetic loci. Each family member can have polymorphism in which nucleotide variation may occur at a given genetic loci. Polymorphism in the nucleic acid sequence may result in amino acid polymorphism, but this is not always the case as the nucleotide code which encodes for the amino acids is degenerate. The nucleic acid sequence coding for Cyn dI, may vary among individual Bermuda grass plants due to natural allelic variation. Any and all such nucleotide variations and resulting amino acid polymorphisms are within the scope of the invention.

A partial nucleic acid sequence coding for Cyn dI, derived from a cDNA clone designated clone 2, has the sequence shown in FIG. 1 (SEQ ID NOS: 1and 2). The partial nucleic acid sequence (SEQ ID NO: 1) coding for Cyn dI shown in FIG. 1 comprises 435 bases. The 3′ untranslated region starts at base 436 and extends to base 662. The deduced partial amino acid sequence (SEQ ID NO: 2) of Cyn dI encoded for by clone 2 (C2) is also shown in FIG. 1 (SEQ ID NO: 1and 2).

FIG. 2 shows the partial nucleic acid (SEQ ID NO: 3) and deduced amino acid sequences (SEQ ID NO: 4) for a second cDNA clone designated clone 18 (C18). The nucleic acid sequence (SEQ ID NO: 3) coding for Cyn dI shown in FIG. 2 comprises 600 nucleotides encoding 200 deduced amino acids. The 3′ untranslated region starts at base 601 and extends to base 775.

As shown in FIG. 3, although the coding sequences for clone 2 (SEQ ID NO: 1) and clone 18 (SEQ ID NO: 3) are clearly homologous, the 3′ untranslated regions are much more divergent. This suggests that clones 2 and 18 may encode separate members of a Cyn dI gene family.

As shown in FIG. 4, the deduced amino acid sequences encoded by clone 2 (SEQ ID NO: 2) and clone 18 (SEQ ID NO: 4) have 88.2% homology (84.1% identity). There are 22 amino acid differences in the 143 amino acid overlap deduced from the two clones of which 6 are conservative substitutions and 16 are non-conservative substitutions. The partial protein encoded by clone 18 (SEQ ID NO: 4) is two amino acids longer at the carboxy terminus than the partial protein encoded by clone 2 (SEQ ID NO: 2) (FIG. 4). Amino acid homology was demonstrated using software contained in PCGENE (Intelligenetics, Mountain View, Calif.).

A comparison of the deduced amino acid sequences encoded by seven cDNA clones derived from the Cyn dI library as described in Example 1 are shown in FIG. 5. (SEQ ID NOS: 2and 4-9) The amino acid sequences encoded by these cDNA clones designated C2, (SEQ ID NO: 2) C3, (SEQ ID NO: 7) C21 (SEQ ID NO: 8), C22, (SEQ ID NO: 5) C23 (SEQ ID NO: 5) and C33 (SEQ ID NO: 9) are shown aligned with the deduced amino acid sequence encoded by clone 18 (C 18) (SEQ ID NO: 4), which is the longest clone derived from the Cyn dI cDNA library. As is shown in FIG. 5 and FIG. 6, the overlapping portion of the amino acid sequences encoded by clones 18 (SEQ ID NO: 4), 22 (SEQ ID NO: 5), 23 (SEQ ID NO: 5), 21 (SEQ ID NO: 8) and 33 (SEQ ID NO: 9) are identical. This suggests that clones 18, 22 (SEQ ID NO: 5), 23 (SEQ ID NO: 5), 21 and 33 are examples of the same Cyn dI gene family member. However, clones 22 and 23 are two amino acids shorter than clone 18 and have different 3′ untranslated regions (FIGS. 2, 16 and 17). This may suggest that clones 22 (SEQ ID NO: 5) and 23 (SEQ ID NO: 5) represent a separate member of the Cyn dI gene family. Alternatively, they could represent differentially spliced forms of the same family member.

As is shown in FIG. 5, there are only five amino acid differences between the deduced amino acid sequences encoded by clones 2 (SEQ ID NO: 2) and 3. (SEQ ID NO: 7) Accordingly, clones 2 and 3 may represent polymorphisms of a Cyn dI gene family member, which Cyn dI gene family member is different from the Cyn dI gene family member(s) to which clones 18, (SEQ ID NO: 4) 21, (SEQ ID NO: 8) and 33 (SEQ ID NO: 3) belong. Assuming that clones 2 (SEQ ID NO: 2) and 3 (SEQ ID NO: 7) do represent polymorphisms of a Cyn dI gene family member, a predicted partial amino acid sequence of Cyn dI designated Cyn dI.2/3 (SEQ ID NO: 16) as shown in FIG. 10 may be generated from the amino acid sequences encoded by clones 2 (SEQ ID NO: 2) and 3 (SEQ ID NO: 7).

FIG. 6 shows the nucleotide sequence of cDNA clone 14a1 (SEQ ID NO: 10) and its deduced amino acid sequence (SEQ ID NO: 11). This clone was isolated from a PCR as described in Example 2 and the amino acid sequence it encodes corresponds to the amino portion of the Cyn dI family member partially encoded by clone 18 (SEQ ID NO: 4). There is a 19 nucleotide overlap between the 3′ (SEQ ID NO: 7) end of clone 14a1 and the 5′ end of clone 18. Clone 14a1 was amplified in the PCR using oligonucleotide primers based on non-coding strand sequence of clone 18, as described in Example 2. The methionine encoded by nucleotides 41-43 of clone 14a1 (SEQ ID NO: 10) presumably represents the first amino acid of the translated protein. This is the first methionine encoded after the in-frame stop codon at nucleotides 11-13 of clone 14a1 (SEQ ID NO: 10) indicating that the initiation of protein translation does not occur 5′ of the methionine encoded by nucleotides 41-43 of clone 14a1 (SEQ ID NO: 10). The nucleotide sequence surrounding the presumptive initiator methionine has a 78% match with the consensus sequence, 5′ AACAATGGC-3′ (Lutcke et al. 1987. EMBO J. 6:43-48), for protein initiation in plants. There is a leader sequence of 22 amino acids before the start of the N-terminus of the mature Cyn dI protein (indicated by amino acid 1 in FIG. 6) (SEQ ID NO: 11), the N-terminus of the mature Cyn dI protein (the first 27 amino acids) having previously been identified (Matthiesen et al., 1988, J. Allergy Clin. Immunol. 81:226; Singh et al., 1990, Monogr. Allergy, 28:101-120; Matthiesen et al., 1991, J. Allergy Clin. Immunol., 88:763-774).

FIG. 7 shows the nucleotide sequence of cDNA clone 14c1 (SEQ ID NO: 12) and its deduced amino acid sequence (SEQ ID NO: 13). This clone was also isolated from a PCR as described in Example 2 and the amino acid sequence it encodes corresponds to the amino portion of the Cyn dI family member partially encoded by clone 18 (SEQ ID NO: 4). This clone is homologous with clone 14a1(SEQ ID NO: 11), but has one amino acid difference with clone 14a1 in the sequence of the mature protein (the N-terminus of the mature Cyn dI protein being indicated by amino acid 1 in FIG. 7) (SEQ ID NO: 13). Clone 14c1 (SEQ ID NOS: 12 and 13) has nucleotide differences in the leader sequence encoding seven amino acid differences with clone 14a1 (SEQ ID NO: 11), including a 12 nucleotide insert that would encode an additional 4 amino acids. A composite sequence of 14a1 and 14c1 including the potential polymorphisms of these clones is designated Cyn d 1.14 (SEQ ID NO: 14) shown in FIG. 8.

The sequences of clones 14a1 (SEQ ID NO: 11) and 14c1 (SEQ ID NO: 13) are useful in generating a predicted full-length nucleic acid sequence encoding Cyn dI. Predicted full-length nucleotide sequences encoding Cyn dI may be derived from the formula:

L₁NYX

wherein L₁ is a nucleic acid sequence of 0-300 nucleotides which includes nucleotides which encode a leader sequence of the Cyn dI protein and which may also include nucleotides of a 5′ untranslated region, N is a nucleic acid sequence comprising up to 600 nucleotides and includes nucleotides which encode the amino terminus portion of mature Cyn dI, Y is that portion of the nucleic acid sequence of clone 2 (SEQ ID NO: 1), clone 18, (SEQ ID NO: 3) clone 3, (SEQ ID NO: 17) clone 22, (SEQ ID NO: 18) or clone 23 (SEQ ID NO: 19) or any polymorphic form of those clones which encodes the mature Cyn dI protein and X is a nucleic acid sequence of 0-600 nucleotides which includes nucleotides of the 3′ untranslated portion of Cyn dI. For example, L₁ may include the nucleic acid sequence represented by nucleotides 1-106 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6 which includes the 5′ untranslated region of clone 14a1 as well as those nucleotides (nucleotides 41-106 as shown in FIG. 6) of clone 14a1 which encode a Cyn dI leader sequence. L₁ may also include the nucleic acid sequence represented by nucleotides 1-103 of clone 14c1 (SEQ ID NO: 12) as shown in FIG. 7 which includes the 5′ untranslated region of clone 14c1 as well as those nucleotides (nucleotides 28-103 as shown in FIG. 7) of clone 14c1 which encode a Cyn dI leader sequence. L₁ may also be a nucleic acid sequence which includes nucleotides of clone 14a1 which encode only the leader sequence portion of Cyn dI (nucleotides 41-106 as shown in FIG. 6) (SEQ ID NO: 10) or the nucleotides of clone 14c1 which encode only the leader sequence portion of Cyn dI (nucleotides 28-103 as shown in FIG. 7) (SEQ ID NO: 12) or any polymorphic form thereof. When one is generating a nucleic acid sequence encoding mature Cyn dI, then L₁ is 0 and X is 0 and the formula then simply is NY. N is preferably the nucleic acid sequence represented by nucleotides 107-244 of clone 14a1 as shown in FIG. 6 or nucleotides 104-243 of clone 14c1 (SEQ ID NO: 12) as shown in FIG. 7, each sequence of which encodes the amino terminus of mature Cyn dI does not overlap the nucleic acid sequence of Y. Y is preferably that portion of the nucleic acid sequence of clone 2, (SEQ ID NO: 1) clone 18, (SEQ ID NO: 3) clone 3, (SEQ ID NO: 17) clone 22, (SEQ ID NO: 18) or clone 23 (SEQ ID NO: 19) which encodes the mature Cyn dI protein and does not represent 3′ untranslated region. For example Y may include nucleotides 1-603 of clone 18 (SEQ ID NO: 3) as shown in FIG. 2, nucleotides 1-594 of clone 22 (SEQ ID NO: 18) as shown in FIG. 16, or nucleotides 1-595 of clone 23 (SEQ ID NO: 19) as shown in FIG. 17. Y may also include nucleotides 1-438 of clone 2 (SEQ ID NO: 1) as shown in FIG. 1, or nucleotides 1-417 of clone 3 (SEQ ID NO: 17) as shown in FIG. 15. X is preferably a nucleic acid sequence which includes nucleotides of the 3′ untranslated portion of clones 2, 3, 18, 22, or 23. For example, X may include nucleotides 604-775 of clone 18 (SEQ ID NO: 3) as shown in FIG. 2, nucleotides 595-802 of clone 22 (SEQ ID NO: 18) as shown in FIG. 16, nucleotides 596-832 of clone 23 (SEQ ID NO: 19) as shown in FIG. 15, nucleotides 439-662 of clone 2 (SEQ ID NO: 1) as shown in FIG. 1 or nucleotides 418-594 of clone 3 (SEQ ID NO: 17) as shown in FIG. 15. As discussed previously, X is 0 when one is generating a nucleic acid sequence encoding mature Cyn dI. Specific examples of composite amino acid sequences of Cyn dI generated from the above-described formula include but are not limited to the following composite sequences: the nucleic acid sequence of L₁ includes nucleotides 1-106 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6 or nucleotides 1-103 of clone 14c1 (SEQ ID NO:12) as shown in FIG. 7, the sequence of N is represented by nucleotides 107-244 of clone 14a1 (SEQ ID NO: 10) or nucleotides 104-243 of clone 14c1 (SEQ ID NO: 12) as shown in FIG. 7. The nucleic acid sequence of Y includes nucleotides 1-603 of clone 18 (SEQ ID NO: 3) as shown in FIG. 2 and the nucleic acid sequence of X includes nucleotides 604-775 of clone 18 (SEQ ID NO: 3) as shown in FIG. 2.

Other predicted composites of full-length amino acid sequences of Cyn dI may be derived from the nucleic acid sequences of the above formula which encodes the full-length or mature Cyn dI protein.

A predicted full-length amino acid sequence for Cyn dI designated Cyn dI.18 (SEQ ID NO: 15) shown in FIG. 9 can be generated by merging the amino acid sequence shown in FIG. 8 designated Cyn dI.14 (SEQ ID NO: 14) with amino acid residues 53-246 of clone 18 (SEQ ID NO: 4) as shown in FIG. 5. The predicted composite of the mature protein in this case, which comprises amino acid 1-246 of Cyn dI.18 (SEQ ID NO: 15) shown in FIG. 9 would have a predicted molecular weight of approximately 26.7 kDa without any post-translational modifications. As used herein, the “mature” Cyn dI protein does not include the amino acid sequence of the leader portion of the Cyn dI protein. In all applicable figures discussed herein, polymorphism or potential polymorphism is shown in superscript and subscript.

A full-length clone was generated using PCR as discussed in Example 3 and as shown in FIGS. 18 and 20 (SEQ ID NOs: 20 and 21). The full-length clone shown in FIG. 18 and designated clone CD1 was generated from a PCR using oligonucleotide primers based on nucleotides 107-125 of clone 14a1 (SEQ ID NO: 10) (FIG. 6) and nucleotides 604-621 of clone 18 (SEQ ID NO: 3) (FIG. 2). The deduced amino acid sequence of clone CD1 (SEQ ID NO: 21) corresponds to the predicted composite full-length amino acid sequence of the Cyn dI protein family member designated Cyn dI18 (SEQ ID NO: 15), as discussed above and as shown in FIG. 9, with the exception of two amino acids. The deduced amino acid sequence of clone CD1 (SEQ ID NO: 21) as shown in FIGS. 18 and 20 is designated Cyn dI.CD1. Cyn dI.CD1 is substantially the same Cyn dI protein as the predicted composite sequence represented by Cyn dI.18 (SEQ ID NO: 15) shown in FIG. 9. A host cell transformed with a vector comprising the cDNA insert of clone CD1 (SEQ ID NO: 20) has been deposited with the ATCC under accession number 69107.

Another predicted composite full-length amino acid sequence designated Cyn dI.2/3 (full-length) (SEQ ID NO: 24) is shown in FIG. 20. Part of this sequence is deduced from a Cyn dI clone which was generated from a PCR using oligonucleotide primers based on nucleotides 178-206 of clone 2 (SEQ ID NO: 1) (FIG. 1) (which is identical to the corresponding nucleotide sequence of clone 3 (SEQ ID NO: 17) (FIG. 15)) and nucleotides essentially identical to nucleotides 107-130 of clone 14a1 (SEQ ID NO: 10) (FIG. 6). This clone was designated clone KAT-39-1. The nucleotide (SEQ ID NO: 22) and deduced amino acid (SEQ ID NO: 23) sequences of clone KAT-39-1 are shown in FIG. 19. The deduced amino acid sequence of clone KAT-39-1 (SEQ ID NO: 23) represents a partial amino acid sequence of Cyn dI that overlaps with part of the predicted amino acid sequence of Cyn dI.2/3 (SEQ ID NO: 16) as shown in FIG. 10. Therefore, the composite sequence formed by combining the nucleic and deduced amino acid sequences of clone KAT-39-1 in conjunction with the nucleic and deduced amino acid sequences of Cyn dI.2/3 represent the nucleic and deduced amino acid sequences of the predicted Cyn dI protein family member composite designated Cyn dI.2/3 (full-length) (SEQ ID NO: 24) as shown in FIG. 20. FIG. 20 shows a comparison of the amino acid sequences of composite sequences designated Cyn dI.18(SEQ ID NO: 15) and Cyn dI.2/3 (full-length) (SEQ ID NO: 24), and the full-length amino acid sequence deduced from the full-length cDNA clone, CD1, designated Cyn dI.CD1 (SEQ ID NO: 21).

Nucleic acids encoding Cyn dI protein allergens as described above may be obtained from any part of Cynodon dactylon plants. Nucleic acids encoding Cyn dI may be obtained from genomic DNA. The nucleic acids coding for Cyn dI may be obtained using the methods disclosed herein or any other suitable technique for isolation and cloning of genes.

Fragments of the nucleic acid sequence coding for fragments of Cyn dI are also within the scope of the invention. Fragments within the scope of the invention include those coding for parts of Cyn dI which induce an immune response in mammals, preferably humans, such as stimulation of minimal amounts of IgE; binding of IgE; eliciting the production of IgG and IgM antibodies; or the eliciting of a T cell response such as proliferation and/or lymphokine secretion and/or the induction of T cell anergy. The foregoing fragments of Cyn dI are referred to herein as antigenic fragments. Fragments within the scope of the invention also include those capable of hybridizing with nucleic acid from other plant species for use in screening protocols to detect allergens that are cross-reactive with Cyn dI. As used herein, a fragment of the nucleic acid sequence coding for Cyn dI refers to a nucleotide sequence having fewer bases than the nucleotide sequence coding for the entire amino acid sequence of Cyn dI and/or mature Cyn dI. Generally, the nucleic acid sequence coding for the fragment or fragments of Cyn dI will be selected from the bases coding for the mature protein, however, in some instances it may be desirable to select all or a part of a fragment or fragments from the leader sequence portion of the nucleic acid sequence of the invention. The nucleic acid sequence of the invention may also contain linker sequences, modified restriction endonuclease sites and other sequences useful for cloning, expression or purification of Cyn dI or fragments thereof.

The present invention provides expression vectors and host cells transformed to express the nucleic acid sequences of the invention. Nucleic acid coding for Cyn dI, or at least one fragment thereof may be expressed in bacterial cells such as E. coli, insect cells (baculovirus), yeast, or mammalian cells such as Chinese hamster ovary cells (CHO). Suitable expression vectors, promoters, enhancers, and other expression control elements may be found in Sambrook et al. Molecular Cloning: A Laboratory Manual, second edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1989). Other suitable expression vectors, promoters, enhancers, and other expression elements are known to those skilled in the art. Expression in mammalian, yeast or insect cells leads to partial or complete glycosylation of the recombinant material and formation of any inter- or intra-chain disulfide bonds. Suitable vectors for expression in yeast include YepSec1 (Baldari et al. (1987) Embo J. 6: 229-234); pMFa (Kurjan and Herskowitz (1982) Cell 30: 933-943); JRY88 (Schultz et al. (1987) Gene 54: 113-123) and pYES2 (Invitrogen Corporation, San Diego, Calif.). These vectors are freely available. Baculovirus and mammalian expression systems are also available. For example, a baculovirus system is commercially available (PharMingen, San Diego, Calif.) for expression in insect cells while the pMSG vector is commercially available (Pharmacia, Piscataway, N.J.) for expression in mammalian cells.

For expression in E. coli, suitable expression vectors include, among others, pTRC (Amann et al. (1988) Gene 69: 301-315); pGEX (Amrad Corp., Melbourne, Australia); pMAL (N.E. Biolabs, Beverly, Mass.); pRIT5 (Pharmacia, Piscataway, N.J.); pET-11d (Novagen, Madison, Wis.) Jameel et al., (1990) J. Virol. 64:3963-3966; and pSEM (Knapp et al. (1990) BioTechniques 8: 280-281). The use of pTRC, and pET-11d, for example, will lead to the expression of unfused protein. The use of pMAL, pRIT5 pSEM and pGEX will lead to the expression of allergen fused to maltose E binding protein (pMAL), protein A (pRIT5), truncated β-galactosidase (PSEM), or glutathione S-transferase (pGEX). When Cyn dI, fragment, or fragments thereof is expressed as a fusion protein, it is particularly advantageous to introduce an enzymatic cleavage site at the fusion junction between the carrier protein and Cyn dI or fragment thereof. Cyn dI or a fragment thereof may then be recovered from the fusion protein through enzymatic cleavage at the enzymatic site and biochemical purification using conventional techniques for purification of proteins and peptides. Suitable enzymatic cleavage sites include those for blood clotting Factor Xa or thrombin for which the appropriate enzymes and protocols for cleavage are commercially available from, for example, Sigma Chemical Company, St. Louis, Mo. and N.E. Biolabs, Beverly, Mass. The different vectors also have different promoter regions allowing constitutive or inducible expression with, for example, IPTG induction (PRTC, Amann et al., (1988) supra; pET-11d, Novagen, Madison, Wiss.) or temperature induction (pRIT5, Pharmacia, Piscataway, N.J.). It may also be appropriate to express recombinant Cyn dI in different E. coli hosts that have an altered capacity to degrade recombinantly expressed proteins (e.g. U.S. Pat. No. 4,758,512). Alternatively, it may be advantageous to alter the nucleic acid sequence to use codons preferentially utilized by E. Coli, where such nucleic acid alteration would not affect the amino acid sequence of the expressed protein.

Host cells can be transformed to express the nucleic acid sequences of the invention using conventional techniques such as calcium phosphate or calcium chloride co-precipitation, DEAE-dextran-mediated transfection, or electroporation. Suitable methods for transforming the host cells may be found in Sambrook et al. supra, and other laboratory textbooks. The nucleic acid sequences of the invention may also be synthesized using standard techniques.

The present invention also provides a method of producing purified Cyn dI or at least one fragment thereof comprising the steps of culturing a host cell transformed with a DNA sequence encoding Cyn dI or at least one fragment thereof in an appropriate medium to produce a mixture of cells and medium containing Cyn dI or at least one fragment thereof; and purifying the mixture to produce substantially pure Cyn dI or at least one fragment thereof. Host cells transformed with an expression vector containing DNA coding for Cyn dI or at least one fragment thereof are cultured in a suitable medium for the host cell. Cyn dI protein and peptides can be purified from cell culture medium, host cells, or both using techniques known in the art for purifying peptides and proteins including ion-exchange chromatography, gel filtration chromatography, ultrafiltration, electrophoresis and immunopurification with antibodies specific for Cyn dI or fragments thereof. The terms isolated and purified are used interchangeably herein and refer to peptides, protein, protein fragments, and nucleic acid sequences substantially free of cellular material or culture medium when produced by recombinant DNA techniques, or chemical precursors or other chemicals when synthesized chemically. Accordingly, an isolated peptide of the invention is produced by recombinant DNA techniques or synthesized chemically and is substantially free of cellular material, culture medium, chemical precursors or other chemicals.

Another aspect of the invention provides preparations comprising Cyn dI or at least one fragment thereof synthesized in a host cell transformed with a DNA sequence encoding all or a portion of Cyn dI, or chemically synthesized, and purified Cyn dI protein, or at least one antigenic fragment thereof produced in a host cell transformed with a nucleic acid sequence of the invention, or chemically synthesized. In preferred embodiments of the invention, the Cyn dI protein is produced in a host cell transformed with the nucleic acid sequence coding for at least the mature Cyn dI protein.

Fragments of Cyn dI can be obtained, for example, by screening peptides synthesized from the corresponding fragment of a nucleic acid sequence of the invention coding for such peptides or synthesized chemically using techniques known in the art. Peptide fragments of the allergen may be obtained by selection of fragments of a desired length with no overlap of the peptides, or selection of overlapping fragments of a desired length, which can be produced recombinantly or synthetically. The fragments can be tested to determine antigenicity (e.g., the ability of the fragment to induce an immune response). Such fragments are referred to herein as antigenic fragments. Fragments of Cyn dI protein allergen which are capable of eliciting a T cell response such as stimulation (i.e., proliferation or lymphokine secretion) and/or are capable of inducing T cell anergy are particularly desirable. Fragments of Cyn dI which do not bind immunoglobulin E (IgE) or bind IgE to a substantially lesser extent than the protein allergen from which the fragments are derived are also particularly desirable. The major complications of standard immunotherapy are systemic responses such as anaphylaxis. Immunoglobulin E is a mediator of anaphylactic reactions which result from the binding and cross-linking of antigen to IgE on mast cells or basophils and the release of mediators (e.g., histamine, serotonin, eosinophil, chemotactic factors). Thus, anaphylaxis could be avoided by the use of a fragment which does not bind IgE, or if the fragment binds IgE, such binding does not result in the release of mediators (e.g., histamine etc.) from mast cells or basophils. In addition, fragments which have minimal IgE stimulating activity are particularly desirable for therapeutic effectiveness. Minimal IgE stimulating activity refers to IgE stimulating activity which is less than the amount of IgE production stimulated by the whole Bermuda grass protein allergen. Preferred fragments of the invention include but are not limited to fragments derived from amino acids 5-246, 10-246, 20-246 and 25-246 of Cyn dI.18 (SEQ ID NO: 15) as shown in FIG. 20; fragments derived from amino acids 5-246, 10-246, 20-246 and 25-246 of Cyn dI.CD1 (SEQ ID NO: 21) as shown in FIG. 20; and fragments derived from amino acids 5-244, 10-244, 20-244 and 25-244 of Cyn dI.2/3 (full-length) (SEQ ID NO: 24) as shown in FIG. 20.

Cyn dI and preferred antigenic fragments thereof, when administered to a Bermuda grass pollen-sensitive individual, are capable of modifying the allergic response of the individual to the allergen, and preferably are capable of modifying the B cell, the T cell response or both the B cell and the T cell response of the individual to the allergen. As used herein, modification of the allergic response of an individual sensitive to a Bermuda grass pollen allergen such as Cyn dI can be defined as non-responsiveness or diminution in symptoms to the allergen, as determined by standard clinical procedures (See e.g., Varney et al., British Medical Journal 302: 265-269 (1990)) including dimunition in Bermuda grass pollen induced asthmatic symptoms. As referred to herein, a dimunition in symptoms includes any reduction in symptoms in the allergic response of an individual to the allergen following a treatment regimen with a protein or peptide of the invention. This dimunition in symptoms may be determined subjectively (i.e., the patient feels more comfortable upon exposure to the allergen), or clinically, such as with a standard test. Initial screening for IgE binding to Cyn dI or fragments thereof may be performed by scratch tests or intradermal skin tests on laboratory animals or human volunteers, or in in vitro systems such as RAST (radioallergosorbent test), RAST inhibition, ELISA assay, radioimmunoassay (RIA), or histamine release.

Antigenic fragments of the present invention which have T cell stimulating activity, and comprise at least one T cell epitope are particularly desirable. T cell epitopes are believed to be involved in initiation and perpetuation of the immune response to a protein allergen which is responsible for the clinical symptoms of allergy. These T cell epitopes are thought to trigger early events at the level of the T helper cell by binding to an appropriate HLA molecule on the surface of an antigen presenting cell and stimulating the relevant T cell subpopulation. These events lead to T cell proliferation, lymphokine secretion, local inflammatory reactions, recruitment of additional immune cells to the site, and activation of the B cell cascade leading to production of antibodies. One isotype of these antibodies, IgE, is fundamentally important to the development of allergic symptoms and its production is influenced early in the cascade of events, at the level of the T helper cell, by the nature of the lymphokines secreted. A T cell epitope is the basic element or smallest unit of recognition by a T cell receptor, where the epitope comprises amino acids essential to receptor recognition and may be contiguous and/or non-contiguous in the amino acid sequence of the protein. Amino acid sequences which mimic those of the T cell epitopes and which modify the allergic response to protein allergens are within the scope of this invention.

Exposure of patients to Cyn dI or to the antigenic fragments of the present invention which comprise at least one T cell epitope may tolerize or anergize appropriate T cell subpopulations such that they become unresponsive to the protein allergen and do not participate in stimulating an immune response upon such exposure. In addition, administration of Cyn dI or an antigenic fragment of the present invention which comprises at least one T cell epitope may modify the lymphokine secretion profile as compared with exposure to the naturally-occurring protein allergen or portion thereof (e.g. result in a decrease of IL-4 and/or an increase in IL-2). Furthermore, exposure to Cyn dI or such antigenic fragment may influence T cell subpopulations which normally participate in the response to the allergen such that these T cells are drawn away from the site(s) of normal exposure to the allergen (e.g., nasal mucosa, skin, and lung) towards the site(s) of therapeutic administration of the fragment. This redistribution of T cell subpopulations may ameliorate or reduce the ability of an individual's immune system to stimulate the usual immune response at the site of normal exposure to the allergen, resulting in a dimunution in allergic symptoms.

Cyn dI and fragments or portions derived therefrom (peptides) can be used in methods of diagnosing, treating and preventing allergic reactions to Bermuda grass pollen. Thus, the present invention provides therapeutic compositions comprising isolated Cyn dI or at least one fragment thereof and a pharmaceutically acceptable carrier or diluent. Cyn dI or at least one fragment thereof is preferably produced in a cell transformed to express the protein allergen or the fragment thereof or is synthetically prepared. Administration of the therapeutic compositions of the present invention to an individual to be desensitized can be carried out using known techniques. Cyn dI or a fragment thereof can be administered to an individual in combination with, for example, an appropriate diluent, a carrier and/or an adjuvant. Pharmaceutically acceptable diluents include saline and aqueous buffer solutions. Pharmaceutically acceptable carriers include polyethylene glycol (Wie et al. (1981) Int. Arch. Allergy Appl. Immunol. 64:84-99) and liposomes (Strejan et al. (1984) J. Neuroimmunol.7: 27). For purposes of inducing T cell anergy, the therapeutic composition is preferably administered in non-immunogenic form, e.g., it does not contain adjuvant. Such compositions will generally be administered by injection (subcutaneous, intravenous etc.), oral administration, inhalation, transdermal application or rectal administration. The therapeutic compositions of the invention are administered to Bermuda grass pollen-sensitive individuals in a treatment regimen at dosages and for lengths of time effective to reduce sensitivity (i.e, reduce the allergic response) of the individual to Bermuda grass pollen. Effective amounts of the therapeutic compositions will vary according to factors such as the degree of sensitivity of the individual to Bermuda grass pollen, the age, sex, and weight of the individual, and the ability of the Bermuda grass pollen allergen or fragment thereof to elicit an antigenic response in the individual.

cDNA coding for a Cyn dI (or the mRNA from which it was transcribed) or a portion thereof can be used to identify similar sequences in any variety or type of plant and thus, to identify or “pull out” sequences which have sufficient homology to hybridize to the cDNA of the protein allergen or mRNA or portion thereof. For example, cDNA of the present invention may hybridize to DNA from temperate grasses such as rye-grass, Kentucky Blue grass, Timothy grass and orchard grass, and from other grasses such as Bahia grass and sorghum, under conditions of low stringency. Those sequences which have sufficient homology (generally greater than 40%) can be selected for further assessment using the method described herein. Alternatively, high stringency conditions can be used. In this manner, DNA of the present invention can be used to identify, in other types of plants, preferably related families, genera, or species, sequences encoding polypeptides having amino acid sequences similar to that of a Cyn dI, and thus to identify allergens in other species. Thus, the present invention includes not only the Bermuda grass allergen Cyn dI, but also other allergens encoded by DNA which hybridizes to DNA of the present invention. The invention further includes isolated protein allergens or fragments thereof, excluding those protein allergens or fragments from the genus Lolium, which are immunologically related to Cyn dI or fragments thereof, such as by antibody cross-reactivity, or other immunological assay wherein the protein allergens or fragments thereof are capable of binding to antibodies specific for Cyn dI or fragments of the invention or by T cell cross-reactivity wherein the isolated allergenic proteins or fragments thereof are capable of stimulating T cells specific for the proteins and peptides of the invention. The invention also includes protein allergens or fragments thereof which have greater than 73% homology with Cyn dI or have greater than 90% homology with Cyn dI.

Proteins or peptides encoded by the cDNA of the present invention can be used, for example as “purified” allergens. Such purified allergens are useful in the standardization of allergen extracts which are key reagents for the diagnosis and treatment of sensitivity to Bermuda grass pollen. Furthermore, by using proteins or fragments thereof based on the nucleic acid sequences of Cyn dI, anti-peptide antisera, polyclonal antibodies or monoclonal antibodies can be made using standard methods. These sera or polyclonal or monoclonal antibodies can be used to standardize allergen extracts and/or used in purification of native or recombinant protein allergens.

Through use of Cyn dI and synthetically or recombinantly produced isolated antigenic fragments thereof, preparations of consistent, well-defined composition and biological activity can be made and administered for therapeutic purposes (e.g. to modify the allergic response of a Bermuda grass pollen-sensitive individual. Administration of such peptides or protein may, for example, modify B-cell response to Cyn dI, T cell response to Cyn dI or both responses. Isolated peptides can also be used to study the mechanism of immunotherapy of Bermuda grass pollen allergy and to design modified derivatives or analogues useful in immunotherapy.

It is possible to modify the structure of Cyn dI or fragments thereof of the invention, for such purposes as increasing solubility, enhancing therapeutic or preventive efficacy, or stability (e.g., shelf life ex vivo, and resistance to proteolytic degradation in vivo). Modified Cyn dI or a modified fragment thereof can be produced in which the amino acid sequence has been altered, such as by amino acid substitution, deletion, or addition, to modify immunogenicity and/or reduce allergenicity, or to which a component has been added for the same purpose. For example, the amino acid residues essential to T cell epitope function can be determined using known techniques (e.g., substitution of each residue and determination of presence or absence of T cell reactivity). Those residues shown to be essential can be modified (e.g., replaced by another amino acid whose presence is shown to enhance T cell reactivity), as can those which are not required for T cell reactivity (e.g., by being replaced by another amino acid whose incorporation enhances T cell reactivity but does not diminish binding to relevant MHC). In order to enhance stability and/or reactivity, Cyn dI or a fragment thereof can also be modified to incorporate one or more polymorphisms in the amino acid sequence of the protein allergen resulting from natural allelic variation. Additionally, D-amino acids, non-natural amino acids or non-amino acid analogues can be substituted or added to produce a modified protein or fragment within the scope of this invention. Furthermore, Cyn dI or fragments thereof can be modified using the polyethylene glycol (PEG) method of A. Sehon and co-workers (Wie et al. supra) to produce a peptide conjugated with PEG. Modifications of Cyn dI or fragments thereof can also include reduction/alkylation (Tarr in: Methods of Protein Microcharac-terization, J. E. Silver ed. Humana Press, Clifton, N.J., pp 155-194 (1986)); acylation (Tarr, supra); esterification (Tarr, supra); chemical coupling to an appropriate carrier (Mishell and Shiigi, eds, Selected Methods in Cellular Immunology, W H Freeman, San Francisco, Calif. (1980); U.S. Pat. No. 4,939,239); or mild formalin treatment (Marsh International Archives of Allergy and Applied Immunology 41: 199-215 (1971)).

Site-directed mutagenesis of DNA encoding Cyn dI or fragment thereof can be used to modify the structure. Such methods may involve PCR (Ho et al., Gene 77:51-59 (1989)) or total synthesis of mutated genes (Hostomsky, Z., et al., Biochem. Biophys. Res. Comm.161:1056-1063 (1989)). To enhance bacterial expression, the aforementioned methods can be used in conjunction with other procedures to change the plant codons in DNA constructs encoding the peptides to ones preferentially used in E. coli.

Using the structural information now available, it is possible to design Cyn dI peptides which, when administered to a Bermuda grass pollen sensitive individual in sufficient quantities, will modify the individual's allergic response to Bermuda grass pollen. This can be done, for example, by examining the structure of Cyn dI and producing peptides (via an expression system or synthetically) to be examined for their ability to influence B cell and/or T cell responses in Bermuda grass pollen sensitive individuals and selecting appropriate B or T cell epitopes recognized by the cells. Protein, peptides or antibodies of the present invention can also be used for detecting and diagnosing sensitivity to Bermuda grass pollen allergens. For example, this could be done by combining blood or blood products obtained from an individual to be assessed for sensitivity to Bermuda grass pollen with an isolated antigenic fragment of Cyn dI, or isolated Cyn dI, under conditions appropriate for binding of components (e.g., antibodies, T cells, B cells) in the blood with the fragment(s) or protein and determining the extent to which such binding occurs.

It is now also possible to design an agent or a drug capable of blocking or inhibiting the ability of Cyn dI to induce an allergic reaction in Bermuda grass pollen sensitive individuals. Such agents could be designed, for example, in such a manner that they would bind to relevant anti-Cyn dI-IgE's, thus preventing IgE-allergen binding and subsequent mast cell degranulation. Alternatively, such agents could bind to cellular components of the immune system, resulting in suppression or desensitization of the allergic response to Bermuda grass pollen. A non-restrictive example of this is the use of appropriate B and T cell epitope peptides, or modifications thereof, based on the cDNA/protein structures of the present invention to suppress the allergic response to Bermuda grass pollen. This can be carried out by defining the structures of B and T cell epitope peptides which affect B and T cell function in in vitro studies with blood components from Bermuda grass pollen sensitive individuals.

The DNA used in any embodiment of this invention can be cDNA obtained as described herein, or alternatively, can be any oligodeoxynucleotide sequence having all or a portion of a sequence represented herein, or their functional equivalents. Such oligodeoxynucleotide sequences can be produced chemically or mechanically, using known techniques. A functional equivalent of an oligonucleotide sequence is one which is capable of hybridizing to a complementary oligonucleotide to which the sequence (or corresponding sequence portions) thereof hybridizes, or the sequence (or corresponding sequence portion) complementary to the nucleic acid sequences, and/or which encodes a product (e.g., a polypeptide or peptide) having the same functional characteristics of the product encoded by the sequence (or corresponding sequence portion). Whether a functional equivalent must meet one or both criteria will depend on its use (e.g., if it is to be used only as an oligoprobe, it need meet only the first criterion and if it is to be used to produce Cyn dI, it need only meet the second criterion).

This invention is further illustrated by the following non-limiting examples.

EXAMPLE 1 Isolation of Cyn dI for Protein Sequencing and MAb Production

Preparation of Pollen Extract

Bermuda grass pollen was purchased from Greer Laboratories, Lenoir, N.C., USA. To prepare the pollen extract of soluble proteins which was loaded on the Rotofor, 5 grams of Bermuda grass pollen was extracted three times by shaking with 10 ml of 10 mM phosphate buffered saline (PBS) for one hour at 4° C. After each extraction, the mixture was centrifuged (2500 rpm, 10 minutes) and the supernatant collected. After three extractions the supernatants were pooled and filtered through a 3 mm Whatman filter.

Preparative Isoelectric Focusing (IEF)

Preparative JEF in the Rotofor (Biorad, Richmond, Calif.) has been described in detail by Egan et al. (1988) Analyt. Biochem, 172, 488-494. Briefly, 5 ml of ampholyte solution (Bio-lyte, pH range 3-10; 40%) was added to the pollen extract and the volume adjusted to 50 ml with distilled water. This mixture was loaded into the Rotofor cell and focussed at 4° C. and 12 W constant power. After four hours, 20 fractions were collected and their pH determined. Fractions containing the proteins of interest were identified with MAb 3.2 on immunoblots after SDS-PAGE. This MAb was raised against purified Lol pI but was found to be cross-reactive with Group I homologues from nine other grasses including Bermuda grass (Kahn and Marsh, 1986, Mol. Immunol., 23, 1281-1288). Fractions containing the proteins of interest were pooled and refractionated in the Rotofor using the same conditions as above except that samples were focussed for 2.5 hours. The pH of each fraction was determined.

SDS-PAGE and Western Blotting

Proteins in Rotofor fractions were separated under reducing conditions by electrophoresis on 10-15% gradient SDS-polyacrylamide gels. Conditions for electrophoresis were essentially as described by Singh and Knox, Int. Archs Appl. Immun., 78, 300-304 (1985). Molecular weights (MW) were determined using low MW standards from Pharmacia. Proteins on polyacrylamide gels were visualized by staining with Coomassie Brilliant Blue R250.

Proteins were transferred to nitrocellulose (Schleicher and Schuell, 0.45 μm) according to Towbin et al. (1979); Proc. Natl. Acad. Sci. U.S.A., 76, 4350-4354; at 120 mA overnight at 4° C. After protein transfer, non-specific binding sites were blocked by incubation of the Western blots in powdered milk [10% in 10 mM TBS (Tris-buffered saline: 150 mM NaCl/10 mM Tris.HCl, pH 7.5)].

Separation by SDS-PAGE of fractions obtained by preparative IEF, revealed that Cyn dI focussed in fractions 10-20 with a pH range of 6-10. These fractions contained 31-32 kD proteins which bound MAb 3.2. The proteins in fractions 10-13 (32 kD) which bound MAb 3.2 had a slightly higher MW than those in fractions 15-20 (31 kD) (FIGS. 11a-b). The intermediate fraction 14 contained both proteins that bound MAb 3.2. These proteins have been designated Cyn dIa (32 kD) and Cyn dIb (31 kD).

Fractions 10-13 of FIG. 11a containing Cyn dIa were pooled and refractionated. Cyn dIa was found in all fractions of FIG. 12a, but dominated the protein component of fractions 13-20 (FIG. 12a). These fractions had a pH of 6.5; an indication of the pI of Cyn dIa.

Fractions 15-20 of FIG. 11a were pooled and refractionated in order to purify Cyn dIb. Cyn dIb was found in all fractions of FIG. 12b but dominated the protein profile of fractions 1-12 (FIG. 12b). These fractions had a pH of 7.4; an indication of the pI of Cyn dIb.

Immunoblot Analysis

Western blots were incubated in MAb 3.2 or in sera of allergic individuals. MAb 3.2 was diluted 1:1000 in PBS containing 0.5% BSA. MAb binding was visualized by incubation in a solution of peroxidase-labelled, anti-mouse Ig antibody (Dakopatts Corporation, Carpinteria, Calif., USA) followed by addition of the enzyme substrate as described by Singh and Knox (1985) supra. Human serum was diluted 1:4 in 150 mM PBS containing 0.5% BSA. IgE binding was visualized by incubation of the blot in ¹²⁵I-labelled anti-human IgE (Kallestad) (diluted 1:6 in PBS/BSA) followed by autoradiography. Purified Cyn dIa and Ib were assessed for their ability to bind to IgE from the serum of allergic individuals (FIG. 13). Both fractions bound IgE from the sera of a Bermuda grass allergic individual.

NH₂-terminal Amino Acid Sequencing

Cyn dI proteins Cyn dIa and Cyn dIb, isolated, as described above, and electrotransfered onto polyvinylidene difluoride (PVDF) membrane (Millipore, Bedford, Mass., USA) using 10 mM CAPS 10% methanol (pH 11.0) as the transfer buffer (Ward et al., 1990) (3 [cyclohexylamino]-1-propane sulfonic acid), were then visualized by staining with Coomassie Brilliant Blue R250, destained in methanol acetic acid water (50:10:40, v/v/v) and washed extensively with deionized water. The NH₂-terminal amino acid sequence of both Cyn dIa (SEQ ID NO: 25) and Cyn dIb (SEQ ID NOS: 26 and 27) proteins was determined as described by Ward et al. (1990);

Cyn dI proteins, isolated by Rotofor, were also purified using reverse-phase HPLC and the NH₂-terminal amino acid sequence of the 31 kD protein determined.

The two Cyn dI components show minor amino acid sequence variations in their NH₂-terminal regions and there is homology between Cyn dI and Lol pI from ryegrass (Table 1).

TABLE 1 NH₂-terminal sequences of Cyn d I isoallergens and Lol p 1. Allergen NH2-terminal amino-acid sequence (SEQ ID NO:25) Cyn d Ia AMG(D)KPGPXITATYGD(K)XL(D)A(K)(T)AF(D) (SEQ ID NO:26) Cyn d Ib + AIGXKPGPXITAXY(G)X(K)XLXA   (D)      (W)      (T) Cyn d Ib* AIGDKPGPXITATYXXKW LDAKATFYGS NP(R) GAA (SEQ ID NO:27) Cyn d I¹ AMGDKPGPXITATYGDKWLDAKAT FYG Cyn d Ia b² AIGDKPGPXITATYGSKXLEAKATFY Cyn d Ic² AMGDKPGPXITAVY Lol pI³ IAKVPPGPNITAEYGDKWLDAKSTWYGKPT + determined after transfer to PVDF membrane; *determined after HPLC purification ¹Matthiesen et al, 1991, supra ²Matthiesen, 1992, et al., European Congress Allergy Clin. Immunol. Conference, Paris, France, May 1992, Abstract. ³Cottam et al., 1986, Biochem. J., 234, 305-310, I.Griffith et al., 1991, FEBS Letters. 279, 210-215; Perez et al., (1990), J.Biol. Chem. 265:16210-16215. ( )tentative designation; X-unknown amino acid.

Production and Screening of MAbs

Anti-Cyn dI MAbs were obtained by intraperitoneal immunization of a Balb/c mouse with 50 μg of Cyn dI (isolated on the Rotofor, Biorad, Richmond, Calif.). RIBI (RIBI Inmunochem, Hamilton, Mont., USA) was used as an adjuvant in the first of four immunizations. The remaining intraperitoneal immunizations were in saline. Fusion and growth of hybridomas was essentially as described by Harlow and Lane 1988, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory. Single cell cloning was by limited dilution. Hybridomas producing anti-Cyn dI antibodies were identified using an ELISA assay. ELISA plates were coated overnight with 60 μg of Bermuda grass pollen extract diluted in CAPS buffer (6.67 mM NaCO₃ 35 mM NaHCO₃ pH 9.6). The wells were then washed three times with TPBS (PBS containing 0.1% Tween 20) and blocked for 30 minutes with PBS containing 1% BSA (PBS/BSA). 100 μL of primary antibody was added to each well and incubated for 60 minutes, followed by washing (as above) and incubation in β-gal labelled anti-mouse Ig (1/250 dilution in PBS/BSA, 60 minutes). After washing 200 μL of the fluorescent substrate 4-methylumbelliferyl-B-D-galactoside (MUG) was added to each well and incubated at 37° C. for 30 minutes. The plates were then read on the fluoroCount 96 flurometer (Pharmacia).

Antibodies which were positive by this method were designated 3A2, 4D2, 1D1 and 3C2 and tested for binding to Cyn dI on a Western blot of Bermuda grass pollen proteins separated by SDS-PAGE.

cDNA Library and Immunological Screening

Poly (A+) mRNA was isolated from Bermuda grass pollen purchased from Greer Laboratories, Lenoir, N.C., USA essentially as described by Herrin and Michaels (1984). cDNA was synthesized using the Pharmacia cDNA synthesis kit and cloned into the Eco RI site of the vector lambda-gt 11. Recombinant proteins from phage plaques were transferred to nitrocellulose filters by overlaying the plated cDNA library with nitrocellulose filters impregnated with IPTG. These filters were then incubated in mixed anti-Cyn dI MAbs. Binding of MAbs to recombinant proteins was visualized as described above. Plaques producing proteins which bound to anti-Cyn dI MAbs were isolated and purified.

Isolation of CDNA Clones

The Bermuda grass pollen cDNA library, as described above, was initially screened with a mixture of anti-Cyn dI hybridoma supernatants containing mainly MAb 3.2 and 30 positive cDNA clones were plaque purified. These clones were then tested for binding to anti-Cyn dI MAbs 3A2, 4D2, 3C2 and 1D1. All clones selected after the first round of screening produced recombinant fusion proteins specific for MAb 3A2. Binding of the clones to MAbs is shown in FIG. 14 and is summarized in Table 2. It is concluded that the cDNA clones isolated here encode Cyn dI based on the MAb binding shown to the recombinant fusion proteins. MAb 1D1 had a much higher background binding than the other MAbs, making its binding much more subjective.

TABLE 2 Monoclonal Antibody Binding Clone 3A2 4D2 3C2 1D1 Size (bp)  1 +  2 + + + 700  3 + + + 650  4 + + + 500  5 +  7 + + +  8 + + + + 13 + 15 + 16 + 18 + + 800 19 + 20 + 21 + 400 22 + + 800 23 + + + + 900 24 + 25 + + 26 + 27 + 28 + 29 + 31 + 32 + 33 + 400 34 + + + 35 + 36 + 37 +

Nucleotide and Amino Acid Sequences of cDNA Clones

Clones 2, 3, 18, 21, 22, 23 and 33 (see Table 2) were chosen for further study on the basis of their antibody affinity. cDNA inserts from clones 2, 3, 18, 21, 22, 23 and 33 were isolated from the phage and subcloned into pGEM-4Z (Promega) or Bluescript (Stratagene) vectors. DNA sequence was determined by double stranded sequencing carried out by the chain termination method (Sanger et al., Proc. Nat'l Acad. Sci., (1977), 74:5460-5463) using T7 polymerase (Pharmacia). The nucleotide and deduced amino acid sequences of these clones are shown in FIG. 1 (clone 2) (SEQ ID NOS: 1 and 2), FIG. 2 (clone 18) (SEQ ID NOS: 3 and 4), FIG. 15 (clone 3), (SEQ ID NOS: 17 and 7) FIG. 16 (clone 22) (SEQ ID NOS: 18 and 5) and FIG. 17 (clone 23) (SEQ ID NOS: 19 and 5).

All clones sequenced show homology with each other, particularly in the open reading frame (ORF). In addition, there is significant nucleotide sequence homology between all clones sequenced and Lol pI, a major allergen of ryegrass. However, the sequenced clones can be separated into three groups on the basis of nucleotide and deduced amino acid sequence homology, those with sequence most similar to clone 2 (i.e., clone 3), those with sequence most similar to clone 18 (i.e., clones 21 and 33), and those most similar to clone 22 (i.e., clone 23). The deduced amino acid sequences encoded by the ORFs of clones 18 (SEQ ID NO: 4) and 2 (SEQ ID NO: 2) were compared to the deduced amino acid sequence of Lol pI (Perez et al, 1991 supra; Griffith et al, 1991, supra)(FIG. 6). There is 67% amino acid homology between Lol pI and clone 18 and 72% between Lol pI and clone 2. The deduced amino acid sequences of clones 2 (SEQ ID NO: 2) and 18 (SEQ ID NO: 4) have 83% identity (87% homology) with each other.

EXAMPLE 2 Cloning the 5′ end of Cyn dI

Double-stranded CDNA was synthesized from approximately 4 μg of pollen RNA (Greer Labs, Lenoir, N.C., USA) using the cDNA Synthesis System Plus kit (BRL, Bethesda, Md., USA). After a phenol extraction and ethanol precipitation, the cDNA was blunted with T4 DNA polymerase (Promega, Madison, Wiss., USA), and ligated to ethanol precipitated, self-annealed, AT, 5′-GGGTCTAGAGGTACCGTCCGATC-GATCATT-3′ (SEQ ID NO: 28), and AL, 5′-p-AATGATCGATGCT-3′ (SEQ ID NO: 29), oligonucleotides for use in a modified Anchored PCR (Marsh et al, 1986: Roux and Dhanarajan, 1990; Rafnar et al, 1991) reaction. cDNA encoding the amino terminus of Cyn dI was amplified from the linkered cDNA (5 μl from a 20 μl reaction) with 1 μg each of oligonucleotides AP, 5′-GGGTCTAGAGGTACCGTCCG-3′ (SEQ ID NO:30), and CD-5, 5′-GATGTGCTCGTAGTTCTT-3′ (SEQ ID NO: 31), an oligonucleotide primer based on non-coding strand sequence of Cyn dI corresponding to the amino acid sequence KNYEHI. The primary polymerase chain reactions (PCR) were carried out in a programmable thermal controller from MJ Research, Inc. (Cambridge, Mass., USA) using the GeneAmp DNA Amplification kit (Perkin Elmer Cetus, Norwalk, Conn., USA) in a reaction containing 10 μl 10× buffer containing dNTPs, 1 μg of each primer, cDNA, 0.5 μl Amplitaq DNA polymerase, and distilled water to 100 μl. Twenty-five rounds of amplification consisted of denaturation at 94° C. for 1 minute, annealing of primers to the template at 65° C. for 1.5 minutes, and chain elongation at 72° C. for 2 minutes. Five percent (5 μl) of this primary amplification was then used in a secondary amplification with 1 μg each of CD-4, 5′-GGGGATCCGAGGCCGTCCYYGAAG-3′ (SEQ ID NO: 33), a Cyn dI oligonucleotide primer nested relative to CD-5 (SEQ ID NO: 31) based on non-coding strand sequence corresponding to amino acids IFKDGL (SEQ ID NO: 34), and AP, (SEQ ID NO: 30) as above. All oligonucleotides were synthesized by Research Genetics, Inc (Huntsville, Ala.). Oligonucleotide primers AP (SEQ ID NO: 30), AT (SEQ ID NO: 28) and AL (SEQ ID NO: 29) have been previously described (Rafnar et al, 1991; Morgenstern et al, 1991; Griffith et al, 1991; Rogers et al, 1991). The first eight nucleotides of CD-4 (SEQ ID NO: 33) were added to create a Bam HI restriction site for cloning purposes.

Amplified DNA was recovered by sequential chloroform, phenol, and chloroform extractions, followed by precipitation at −20° C. with 0.5 volumes of 7.5 ammonium acetate and 1.5 volumes of isopropanol. After precipitation and washing with 70% ethanol, the DNA was simultaneously digested with Xba I and Bam HI in a 15 μl reaction and electrophoresed through a preparative 3% SeaPlaque low melt agarose gel (FMC Corp., Rockland Me., USA). The appropriate sized DNA band was visualized by ethidium bromide (EtBr) staining, excised, and ligated into appropriately digested M13mpl9 for dideoxy DNA sequencing (Sanger et al, (1977), Proc. Nat'l. Acad. Sci USA,74:5460-5463) with the Sequenase kit (U.S. Biochemicals, Cleveland, Ohio, USA). Two clones, 14a1 (SEQ ID NO: 10) and 14c1 (SEQ ID NO: 12), were obtained from this ligation, completely sequenced and found to contain in-frame initiator methionines. The methionine encoded by nucleotides 28-30 of the 14a1 (SEQ ID NO: 10) sequence (FIG. 6) most preferably represents the initiating codon since the surrounding sequence closely matches the common plant sequence, 5′-AACAATGGC-3′ (Lutcke at al, (1987) Embo. J., 6:43-48), and there is an in-frame stop codon just upstream. Although 14c1 (SEQ ID NO: 12) (FIG. 7) contained two potential in-frame methionines, the methionine encoded by nucleotides 27-29 is most probably the initiator methionine since the surrounding sequence more closely matches the consensus plant sequence, 5′-AACAATGGC-3′ (Lutcke at al, supra), than does the methionine encoded by nucleotides 42-45 (78% vs. 56% match). Furthermore, the sequence surrounding nucleotides 27-29 is identical to that of clone 14a1. Both clone 14a1 (SEQ ID NO: 10) and clone 14c1 (SEQ ID NO: 12) sequences had 17 nucleotide overlaps with the longest Cyn dI clone, clone 18(SEQ ID NO: 3). The amino terminus of the mature Cyn dI NH₂-AIGDKPGPNITATGNKWLEAKATFYG (SEQ ID NO: 35) encoded by clone 14a1 (SEQ ID NO: 10) and NH2-AIGDKPGPNITATGSKWLEAKATFYG- (SEQ ID NO: 36) encoded by clone 14c1 could be identified by comparison with two previously published protein sequences for Cyn dI: NH2-AMGDKPGP?ITATYGDKWLDAKATFYG (SEQ ID NO: 41) (Matthiesen et al, 1988, supra; Matthiesen et al, 1990, supra; Matthiesen et al, 1991, supra) and NH2-AIGDKPGPKITATY??KWLEAKAT (SEQ ID NO: 45) (Singh et al, 1990, supra). This indicated that clones 14a1 and 14c1 had leader sequences of 22 and 26 amino acids, respectively. These leader sequences would be cleaved to create the mature form of the Cyn dI protein. The potential full-length amino acid sequence of Cyn dI designated Cyn dI.18 (SEQ ID NO:15) (FIG. 9) was created by attaching the sequence of Cyn dI.14 (SEQ ID NO: 14) to clone 18 (SEQ ID NO: 4) at their overlap as shown in FIG. 9. In both cases, the mature form of Cyn dI is predicted to be 246 amino acids with a calculated molecular weight of 26.7 kDa.

EXAMPLE 3

RNA was isolated from the pollen of Cynodon dactylon using a modification of the guanidinium thiocyanate method of Chomczynski and Sacchi (1987) Analytical Biochem. 162: 156-159. Pollen was ground in liquid nitrogen with 9 mls of guanidinium thiocyanate buffer (5 M guanidinium thiocyanate in 0.05% Tris-HCl [pH 7.0], 0.05 vol. β-mercaptoethanol, 0.1 vol. 5% sodium lauroyl sarkosine). The pollen solution was then shaken with phenol (10 ml) for 10 min, after which 10 ml of chloroform:isoamyl alcohol 24:1 was added and the mixture shaken for a further 20 min. The mixture was centrifuged at 7,000×g for 25 min and the aqueous phase collected.

The aqueous phase was re-extracted with phenol:chloroform:isoamyl alcohol 25:24:1 followed by centrifugation at 2,000×g until the interface was clear. The aqueous phase was then decanted into a quickseal ultracentrifuge tube, underlain with a 3 ml CsCl cushion (5.7 M CsCl in 0.1 M EDTA; density=1.71 g/ml) and centrifuged (20 hrs, 40,000 rpm, 20° C.) in a Beckman Ti 70.1 rotor (Beckman L8-70 ultracentrifuge; Beckman Instruments, Fullerton, Calif.). After centrifugation, RNA in the pellet was resuspended in 0.05% SDS, phenol/chloroform extracted and ethanol precipitated overnight at −20° C.

Poly A⁺ RNA was isolated using a Pharmacia mRNA Purification kit (Pharmacia, Piscataway, N.J.), following the manufacturers instructions.

First strand cDNA was prepared by heating 0.8 μg mRNA to 70° C. with 0.5 μg of oligo-dT primer (Pharmacia, Piscataway, N.J.). After the mRNA solution was cooled on ice, 5× first strand buffer and 25U RNAsin ribonuclease inhibitor were added. The mixture was then heated at 42° C. for 1 hr. Final reaction conditions were 50 mM Tris-HCl, pH 8.3, 50 mM KCl, 10 mM MgCl₂, 0.5 mM spermidine, 10 mM DTT, 4 mM sodium pyrophosphate, 1 mM each of dATP, dCTP, dGTP, and TTP, 25U RNAsin ribonuclease inhibitor and 15u AMV reverse transcriptase/μg RNA (Promega cDNA synthesis kit, Promega, Madison, Wiss.) in a final volume of 25 μl. cDNA sequences encoding Cyn dI were amplified using the Perkin-Elmer Cetus gene amplification kit (U.S. Biochemicals, Cleveland, Ohio). 5 μl (25%) of the first strand cDNA synthesis product was mixed with 10× buffer to a final buffer concentration of 2 mM MgCl₂, 50 mM KCl, 10 mM Tris-HCl, 1 μg of oligonucleotide primer CDI5′N, 5′-GGGAATTCGCCATCGGCG-ACAAG-CCAG-3′ (SEQ ID NO: 37), 1 μg of oligonucleotide primer CDI3′B18, 5′-CCCTGCAGATG-GAGGATCATCGTCTC-3′ (SEQ ID NO: 38), 0.2 mM dNTP and 2.5 units of Taq DNA polymerase (Pharmacia, Piscataway, N.J.). Nucleotides 1-8 of CDI5′N (SEQ ID NO: 37) were added to create an Eco RI endonuclease restriction site for cloning purposes, while nucleotides 9-27 correspond to nucleotides 107 to 125 of clone 14a1 (SEQ ID NO: 10) in FIG. 6 that encode amino acids 1-6 (AIGDKP) of Cyn dI (Table I, FIGS. 8 and 9). Nucleotides 1-8 of CDI3′B18 were added to create a Pst I endonuclease restriction site for cloning purposes, while nucleotides 9-26 correspond to non-coding strand sequence complementary to nucleotides 604 to 621 of clone 18 (SEQ ID NO: 3) (FIG. 2).

The PCR was performed in a Perkin-Elmer Cetus Thermal Cycler (Perkin-Elmer, Norwalk, Conn.) and consisted of 5 cycles of denaturation (94° C., 1 min), annealing (45° C., 1.5 min), and elongation (72° C., 3 min) followed by 20 cycles of denaturation (94° C., 1 min), annealing (55° C., 1.5 min), and elongation (72° C., 3 min). The final elongation reaction was performed at 72° C. for 10 min. Amplified product was recovered by phenol extraction, chloroform extraction, and then precipitation at −20° C. with 0.5 vol 7.5 M ammonium acetate and 1.5 volumes isopropanol. Reaction product was blunted with Klenow fragment of DNA polymerase then cut with Eco RI and cloned into Bluescript vector digested with Eco RI and Hin cII. The clone CD1 was sequenced by the dideoxy chain termination method (Sanger, supra.), as described in Example 1, and found to contain the nucleotide and deduced amino acid sequences of Cyn dI shown in FIG. 18 (SEQ ID NOS: 20 and 21).

EXAMPLE 4

Double stranded cDNA was prepared and amplified using oligonucleotide primers CD-13 (SEQ ID NO: 39) and CD-15 (SEQ ID NO: 40) in a primary PCR reaction as described in Example 2. CD-13 has the sequence 5′-TTTCTAGAGCCATCGGCGACAAGCCAGGGCCC-3′ (SEQ ID NO: 39), whereas nucletoide 14 could be C or G. Nucleotides 1 through 8 of CD-13 (SEQ ID NO: 39) (5′-TTTCTAGA-3′) were added to create a Xba I restriction site for cloning purposes. The remaining nucleotides encoded amino acids Ala(Ile/Met)-GlyAspLysProGlyPro, where amino acid 2 could be either Ile or Met (amino acids 1 through 8 of Cyn dIa (SEQ ID NO: 25) and Cyn dIb (SEQ ID NO: 27) (Table I). CD-15 has the sequence 5′-GCGTACTTCACGAGCAGCGCCAG-GTAATT-3′ (SEQ ID NO: 40), which corresponds to non-coding strand sequence complementary to coding strand sequence that encodes amino acids AsnTyrLeuAlaLeuLeuValLysTyrAla (numbered amino acids 159 through 168 of clone 2 (C2) (SEQ ID NO: 2) and clone 3 (C3) (SEQ ID NO: 7) in FIG. 5). Five percent of the primary reaction was amplified in a secondary PCR, as described in Example 2, using oligonucleotide primers CD-13 (SEQ ID NO: 39) and CD-16. CD-16 has the sequence 5′-TTGAATTCGACACGGCGGAACTGCAGCAT-3′ (SEQ ID NO: 6), where nucleotide 12 could be G or A. Nucleotides 1 through 8 of CD-16 (SEQ ID NO: 6) were added to create an Eco RI restriction site for cloning purposes. Nucleotides 9 through 29 corresponded to non-coding strand sequence complementary to coding strand sequence that encode amino acids MetLeuGlnPheArgArgVal (numbered amino acids 132 through 138 of C2 (SEQ ID NO: 2) and C3 (SEQ ID NO: 7) in FIG. 5).

The PCR amplifications were performed as described in Example 2. Amplified product was recovered, appropriately digested and ligated into pUC for sequencing as described in Example 2. A clone, designated KAT-39-1, was isolated that had sequence identifying it as a Cyn dI clone. The nucleotide and deduced amino acid sequences of clone KAT-39-1 are shown in FIG. 19 (SEQ ID NOS: 22 and 23). This clone is an extension of the Cyn dI clones C2 (SEQ ID NO: 1) and C3 (SEQ ID NO: 17). Oligonucleotides CD-15 (SEQ ID NO: 40) and CD-16 (SEQ ID NO: 6) have single nucleotide mismatches at their 3′ ends with the corresponding sequence in Cyn dI clone C 18 (SEQ ID NO: 3) and its homologues. Therefore, only clone C2 or C3, or a close family member would be amplified. A composite sequence of KAT-39-1 (SEQ ID NO: 23) and Cyn dI.2/3 (SEQ ID NO: 16) designated Cyn dI.2/3 (full-length) (SEQ ID NO: 24), is shown in FIG. 20 in comparison to Cyn dI.CD1 (SEQ ID NO: 21) and Cyn dI.18 (SEQ ID NO: 15).

Although the invention has been described with reference to its preferred embodiments, other embodiments can achieve the same results. Variation and modifications to the present invention will be obvious to those skilled in the art and it is intended to cover in the appended claims all such modifications and equivalents that follow in the true spirit and scope of this invention.

45 662 base pairs nucleic acid single linear cDNA CDS 1..435 1 CAC ATT GCT GCC TAC CAC TTC GAC CTC TCC GGC AAA GCC TTC GGC GCC 48 His Ile Ala Ala Tyr His Phe Asp Leu Ser Gly Lys Ala Phe Gly Ala 1 5 10 15 ATG GCC AAG AAG GGA GAG GAG GAC AAG CTG CGC AAG GCC GGC GAA CTG 96 Met Ala Lys Lys Gly Glu Glu Asp Lys Leu Arg Lys Ala Gly Glu Leu 20 25 30 ATG CTG CAG TTC CGC CGT GTC AAG TGC GAG TAC CCA TCC GAC ACC AAG 144 Met Leu Gln Phe Arg Arg Val Lys Cys Glu Tyr Pro Ser Asp Thr Lys 35 40 45 ATC GCC TTC CAC GTC GAG AAG GGC TCA AGC CCC AAT TAC CTG GCG CTG 192 Ile Ala Phe His Val Glu Lys Gly Ser Ser Pro Asn Tyr Leu Ala Leu 50 55 60 CTC GTG AAG TAC GCT GCC GGC GAT GGC AAC ATT GTC GGT GTC GAC ATC 240 Leu Val Lys Tyr Ala Ala Gly Asp Gly Asn Ile Val Gly Val Asp Ile 65 70 75 80 AAG CCC AAG GGC TCC GAC GAG TTC CTG CCC ATG AAG CAG TCG TGG GGC 288 Lys Pro Lys Gly Ser Asp Glu Phe Leu Pro Met Lys Gln Ser Trp Gly 85 90 95 GCC ATC TGG AGG ATC GAC CCC CCC AAG CCA CTT AAG GGT CCC TTC ACC 336 Ala Ile Trp Arg Ile Asp Pro Pro Lys Pro Leu Lys Gly Pro Phe Thr 100 105 110 ATC CGC CTC ACC AGT GAG AGT GGC GGC CAT GTC GAA CAG GAC GAT GTC 384 Ile Arg Leu Thr Ser Glu Ser Gly Gly His Val Glu Gln Asp Asp Val 115 120 125 ATC CCC GAA GAC TGG AAG CCC GAC ACC GTC TAC AAG TCC AAG ATC CAG 432 Ile Pro Glu Asp Trp Lys Pro Asp Thr Val Tyr Lys Ser Lys Ile Gln 130 135 140 TTC TGAGCATTGA TGTGCCCGGA ATTATCGTCC ACGCGATATA ACCCAGCCAT 485 Phe 145 GAGTTTGTGG TATCTTTTTA CTTTTCTTAT TCTTTTTTGC AAGAAAGGGT TTACGGAATA 545 TGCATGCATG CCATATCTAA CAAGCATGCA TGCTTTTCTC TCCTTTTTTT CTACTATTAT 605 TGCATCTCCA CAATTCCATG TGGAGAGTTT TGATGAACAA CAAGGTATAC TCGTGCC 662 145 amino acids amino acid linear protein 2 His Ile Ala Ala Tyr His Phe Asp Leu Ser Gly Lys Ala Phe Gly Ala 1 5 10 15 Met Ala Lys Lys Gly Glu Glu Asp Lys Leu Arg Lys Ala Gly Glu Leu 20 25 30 Met Leu Gln Phe Arg Arg Val Lys Cys Glu Tyr Pro Ser Asp Thr Lys 35 40 45 Ile Ala Phe His Val Glu Lys Gly Ser Ser Pro Asn Tyr Leu Ala Leu 50 55 60 Leu Val Lys Tyr Ala Ala Gly Asp Gly Asn Ile Val Gly Val Asp Ile 65 70 75 80 Lys Pro Lys Gly Ser Asp Glu Phe Leu Pro Met Lys Gln Ser Trp Gly 85 90 95 Ala Ile Trp Arg Ile Asp Pro Pro Lys Pro Leu Lys Gly Pro Phe Thr 100 105 110 Ile Arg Leu Thr Ser Glu Ser Gly Gly His Val Glu Gln Asp Asp Val 115 120 125 Ile Pro Glu Asp Trp Lys Pro Asp Thr Val Tyr Lys Ser Lys Ile Gln 130 135 140 Phe 145 775 base pairs nucleic acid single linear cDNA CDS 1..600 3 GTC GAC AAG CCT CCC TTC GAC GGC ATG ACC GCC TGC GGC AAC GAG CCC 48 Val Asp Lys Pro Pro Phe Asp Gly Met Thr Ala Cys Gly Asn Glu Pro 1 5 10 15 ATC TTC AAG GAC GGC CTC GGC TGC GGC GCA TGC TAC GAG ATC AAG TGC 96 Ile Phe Lys Asp Gly Leu Gly Cys Gly Ala Cys Tyr Glu Ile Lys Cys 20 25 30 AAG GAA CCC GTC GAG TGC TCC GGC GAG CCC GTC CTC GTC AAG ATC ACC 144 Lys Glu Pro Val Glu Cys Ser Gly Glu Pro Val Leu Val Lys Ile Thr 35 40 45 GAC AAG AAC TAC GAG CAC ATC GCC GCC TAC CAC TTC GAC CTC TCC GGC 192 Asp Lys Asn Tyr Glu His Ile Ala Ala Tyr His Phe Asp Leu Ser Gly 50 55 60 AAG GCC TTC GGC GCC ATG GCC AAG AAG GGC CAG GAA GAC AAG CTG CGC 240 Lys Ala Phe Gly Ala Met Ala Lys Lys Gly Gln Glu Asp Lys Leu Arg 65 70 75 80 AAG GCC GGT GAG CTG ACT CTG CAG TTC CGC CGC GTC AAG TGC AAG TAC 288 Lys Ala Gly Glu Leu Thr Leu Gln Phe Arg Arg Val Lys Cys Lys Tyr 85 90 95 CCC TCC GGC ACC AAG ATC ACC TTC CAC ATC GAG AAG GGA TCC AAC GAC 336 Pro Ser Gly Thr Lys Ile Thr Phe His Ile Glu Lys Gly Ser Asn Asp 100 105 110 CAT TAC CTG GCG CTG CTC GTC AAG TAC GCC GCC GGC GAT GGC AAC ATT 384 His Tyr Leu Ala Leu Leu Val Lys Tyr Ala Ala Gly Asp Gly Asn Ile 115 120 125 GTC GCC GTC GAC ATC AAG CCC AAG GAC TCC GAC GAG TTC ATT CCC ATG 432 Val Ala Val Asp Ile Lys Pro Lys Asp Ser Asp Glu Phe Ile Pro Met 130 135 140 AAG TCG TCC TGG GGC GCC ATC TGG AGG ATC GAC CCC AAG AAG CCG CTC 480 Lys Ser Ser Trp Gly Ala Ile Trp Arg Ile Asp Pro Lys Lys Pro Leu 145 150 155 160 AAG GGC CCC TTC TCC ATC CGC CTC ACC TCC GAG GGC GGC GCC CAT CTC 528 Lys Gly Pro Phe Ser Ile Arg Leu Thr Ser Glu Gly Gly Ala His Leu 165 170 175 GTC CAG GAC GAC GTC ATC CCA GCC AAC TGG AAG CCA GAC ACC GTC TAC 576 Val Gln Asp Asp Val Ile Pro Ala Asn Trp Lys Pro Asp Thr Val Tyr 180 185 190 ACC TCC AAG CTC CAG TTC GGA GCC TGAGAGACGA TGATCCTCCA TGCATATCCT 630 Thr Ser Lys Leu Gln Phe Gly Ala 195 200 CGCCGATTGC AAGGGCTCAT ATATGACATG TGCGTGTACG CATCTGTCGA ATAAGCATCC 690 ATATATGCAT GAGTTTAATA TTTCTTTTTA TTTCCCCCCT TCAATTATAT GTACATCTCA 750 ATGTGGAGAG TTATTTTCTC GTGCC 775 200 amino acids amino acid linear protein 4 Val Asp Lys Pro Pro Phe Asp Gly Met Thr Ala Cys Gly Asn Glu Pro 1 5 10 15 Ile Phe Lys Asp Gly Leu Gly Cys Gly Ala Cys Tyr Glu Ile Lys Cys 20 25 30 Lys Glu Pro Val Glu Cys Ser Gly Glu Pro Val Leu Val Lys Ile Thr 35 40 45 Asp Lys Asn Tyr Glu His Ile Ala Ala Tyr His Phe Asp Leu Ser Gly 50 55 60 Lys Ala Phe Gly Ala Met Ala Lys Lys Gly Gln Glu Asp Lys Leu Arg 65 70 75 80 Lys Ala Gly Glu Leu Thr Leu Gln Phe Arg Arg Val Lys Cys Lys Tyr 85 90 95 Pro Ser Gly Thr Lys Ile Thr Phe His Ile Glu Lys Gly Ser Asn Asp 100 105 110 His Tyr Leu Ala Leu Leu Val Lys Tyr Ala Ala Gly Asp Gly Asn Ile 115 120 125 Val Ala Val Asp Ile Lys Pro Lys Asp Ser Asp Glu Phe Ile Pro Met 130 135 140 Lys Ser Ser Trp Gly Ala Ile Trp Arg Ile Asp Pro Lys Lys Pro Leu 145 150 155 160 Lys Gly Pro Phe Ser Ile Arg Leu Thr Ser Glu Gly Gly Ala His Leu 165 170 175 Val Gln Asp Asp Val Ile Pro Ala Asn Trp Lys Pro Asp Thr Val Tyr 180 185 190 Thr Ser Lys Leu Gln Phe Gly Ala 195 200 197 amino acids amino acid linear peptide internal 5 Asp Lys Pro Pro Phe Asp Gly Met Thr Ala Cys Gly Asn Glu Pro Ile 1 5 10 15 Phe Lys Asp Gly Leu Gly Cys Gly Ala Cys Tyr Glu Ile Lys Cys Lys 20 25 30 Glu Pro Val Glu Cys Ser Gly Glu Pro Val Leu Val Lys Ile Thr Asp 35 40 45 Lys Asn Tyr Glu His Ile Ala Ala Tyr His Phe Asp Leu Ser Gly Lys 50 55 60 Ala Phe Gly Ala Met Ala Lys Lys Gly Gln Glu Asp Lys Leu Arg Lys 65 70 75 80 Ala Gly Glu Leu Thr Leu Gln Phe Arg Arg Val Lys Cys Lys Tyr Pro 85 90 95 Ser Gly Thr Lys Ile Thr Phe His Ile Glu Lys Gly Ser Asn Asp His 100 105 110 Tyr Leu Ala Leu Leu Val Lys Tyr Ala Ala Gly Asp Gly Asn Ile Val 115 120 125 Ala Val Asp Ile Lys Pro Lys Asp Ser Asp Glu Phe Ile Pro Met Lys 130 135 140 Ser Ser Trp Gly Ala Ile Trp Arg Ile Asp Pro Lys Lys Pro Leu Lys 145 150 155 160 Gly Pro Phe Ser Ile Arg Leu Thr Ser Glu Gly Gly Ala His Leu Val 165 170 175 Gln Asp Asp Val Ile Pro Ala Asn Trp Lys Pro Asp Thr Val Tyr Thr 180 185 190 Ser Lys Leu Gln Phe 195 29 base pairs nucleic acid single linear cDNA 6 TTGAATTCGA CACGGCGGAA CTGCAGCAT 29 138 amino acids amino acid linear peptide internal 7 Asp Leu Ser Gly Lys Ala Phe Gly Ala Met Ala Lys Lys Gly Glu Glu 1 5 10 15 Asp Lys Leu Arg Lys Ala Gly Glu Leu Met Leu Gln Phe Arg Arg Val 20 25 30 Lys Cys Glu Tyr Pro Ser Asp Thr Lys Ile Ala Phe His Val Glu Lys 35 40 45 Gly Ser Asn Pro Asn Tyr Leu Ala Leu Leu Val Lys Tyr Ala Ala Gly 50 55 60 Asp Gly Asn Ile Val Ser Val Asp Ile Lys Ser Lys Gly Ser Asp Asp 65 70 75 80 Phe Leu Pro Met Lys Gln Ser Trp Gly Ala Ile Trp Arg Ile Asp Pro 85 90 95 Pro Lys Pro Leu Lys Gly Pro Phe Thr Ile Arg Leu Thr Ser Glu Ser 100 105 110 Gly Gly His Val Glu Gln Glu Asp Val Ile Pro Glu Asp Trp Lys Pro 115 120 125 Asp Thr Val Tyr Lys Ser Lys Ile Gln Phe 130 135 86 amino acids amino acid linear peptide internal 8 Leu Ala Leu Leu Val Lys Tyr Ala Ala Gly Asp Gly Asn Ile Val Ala 1 5 10 15 Val Asp Ile Lys Pro Lys Asp Ser Asp Glu Phe Ile Pro Met Lys Ser 20 25 30 Ser Trp Gly Ala Ile Trp Arg Ile Asp Pro Lys Lys Pro Leu Lys Gly 35 40 45 Pro Phe Ser Ile Arg Leu Thr Ser Glu Gly Gly Ala His Leu Val Gln 50 55 60 Asp Asp Val Ile Pro Ala Asn Trp Lys Pro Asp Thr Val Tyr Thr Ser 65 70 75 80 Lys Leu Gln Phe Gly Ala 85 68 amino acids amino acid linear peptide internal 9 Ile Lys Pro Lys Asp Ser Asp Glu Phe Ile Pro Met Lys Ser Ser Trp 1 5 10 15 Gly Ala Ile Trp Arg Ile Asp Pro Lys Lys Pro Leu Lys Gly Pro Phe 20 25 30 Ser Ile Arg Leu Thr Ser Glu Gly Gly Ala His Leu Val Gln Asp Asp 35 40 45 Val Ile Pro Ala Asn Trp Lys Pro Asp Thr Val Tyr Thr Ser Lys Leu 50 55 60 Gln Phe Gly Ala 65 263 base pairs nucleic acid single linear cDNA CDS 41..262 10 ATTGATCATT GGAATCCATT ACATACAGAA GCAGCAAGAA ATG GCG CAC ACG AAA 55 Met Ala His Thr Lys 1 5 CTG GCG CTG GTT GCG GTG CTT GTG GCT GCG ATG GTG GCC GGG CGG GTC 103 Leu Ala Leu Val Ala Val Leu Val Ala Ala Met Val Ala Gly Arg Val 10 15 20 GTG GCC ATC GGC GAC AAG CCA GGG CCC AAC ATC ACG GCG ACC TAC GGC 151 Val Ala Ile Gly Asp Lys Pro Gly Pro Asn Ile Thr Ala Thr Tyr Gly 25 30 35 AAC AAG TGG CTG GAG GCC AAG GCC ACT TTC TAC GGT AGC AAC CCA CGC 199 Asn Lys Trp Leu Glu Ala Lys Ala Thr Phe Tyr Gly Ser Asn Pro Arg 40 45 50 GGT GCC GCC CCC GAT GAC CAC GGC GGC GCT TGC GGG TAC AAG GAC GTC 247 Gly Ala Ala Pro Asp Asp His Gly Gly Ala Cys Gly Tyr Lys Asp Val 55 60 65 GAC AAG CCT CCC TTC G 263 Asp Lys Pro Pro Phe 70 74 amino acids amino acid linear protein 11 Met Ala His Thr Lys Leu Ala Leu Val Ala Val Leu Val Ala Ala Met 1 5 10 15 Val Ala Gly Arg Val Val Ala Ile Gly Asp Lys Pro Gly Pro Asn Ile 20 25 30 Thr Ala Thr Tyr Gly Asn Lys Trp Leu Glu Ala Lys Ala Thr Phe Tyr 35 40 45 Gly Ser Asn Pro Arg Gly Ala Ala Pro Asp Asp His Gly Gly Ala Cys 50 55 60 Gly Tyr Lys Asp Val Asp Lys Pro Pro Phe 65 70 262 base pairs nucleic acid single linear cDNA CDS 28..261 12 GTCCGATCGA TCATTCACAA GCAAGAA ATG GCG CAG ACC ACG ATG AAT CAG 51 Met Ala Gln Thr Thr Met Asn Gln 1 5 AAA CTG GCG CTG GTT GCG TGG CCC GTG GCT GCG ATG GTG GCC GGG CGG 99 Lys Leu Ala Leu Val Ala Trp Pro Val Ala Ala Met Val Ala Gly Arg 10 15 20 GTC GTG GCC ATC GGC GAC AAG CCA GGG CCC AAC ATC ACA GCG ACC TAC 147 Val Val Ala Ile Gly Asp Lys Pro Gly Pro Asn Ile Thr Ala Thr Tyr 25 30 35 40 GGC AGC AAG TGG CTG GAG GCC AAG GCC ACC TTC TAC GGC AGC AAC CCG 195 Gly Ser Lys Trp Leu Glu Ala Lys Ala Thr Phe Tyr Gly Ser Asn Pro 45 50 55 CGC GGT GCC GCC CCC GAT GAC CAC GGC GGC GCT TGC GGG TAC AAG GAC 243 Arg Gly Ala Ala Pro Asp Asp His Gly Gly Ala Cys Gly Tyr Lys Asp 60 65 70 GTC GAC AAG CCT CCC TTC G 262 Val Asp Lys Pro Pro Phe 75 78 amino acids amino acid linear protein 13 Met Ala Gln Thr Thr Met Asn Gln Lys Leu Ala Leu Val Ala Trp Pro 1 5 10 15 Val Ala Ala Met Val Ala Gly Arg Val Val Ala Ile Gly Asp Lys Pro 20 25 30 Gly Pro Asn Ile Thr Ala Thr Tyr Gly Ser Lys Trp Leu Glu Ala Lys 35 40 45 Ala Thr Phe Tyr Gly Ser Asn Pro Arg Gly Ala Ala Pro Asp Asp His 50 55 60 Gly Gly Ala Cys Gly Tyr Lys Asp Val Asp Lys Pro Pro Phe 65 70 75 78 amino acids amino acid linear peptide internal Modified-site /note= “Xaa is an unknown amino acid” Modified-site 5-8 /note= “Xaa is an unknown amino acid” Modified-site 15-16 /note= “Xaa is an unknown amino acid” Modified-site 42 /note= “Xaa is an unknown amino acid” Modified-site 71-72 /note= “Xaa is an unknown amino acid” 14 Met Ala Xaa Thr Xaa Xaa Xaa Xaa Lys Leu Ala Leu Val Ala Xaa Xaa 1 5 10 15 Val Ala Ala Met Val Ala Gly Arg Val Val Ala Ile Gly Asp Lys Pro 20 25 30 Gly Pro Asn Ile Thr Ala Thr Tyr Gly Xaa Lys Trp Leu Glu Ala Lys 35 40 45 Ala Thr Phe Tyr Gly Ser Asn Pro Arg Gly Ala Ala Pro Asp Asp His 50 55 60 Gly Gly Ala Cys Gly Tyr Xaa Xaa Val Asp Lys Pro Pro Phe 65 70 75 272 amino acids amino acid linear peptide internal Modified-site /note= “Xaa is an unknown amino acid” Modified-site 5-8 /note= “Xaa is an unknown amino acid” Modified-site 15-16 /note= “Xaa is an unknown amino acid” Modified-site 42 /note= “Xaa is an unknown amino acid” Modified-site 71-72 /note= “Xaa is an unknown amino acid” 15 Met Ala Xaa Thr Xaa Xaa Xaa Xaa Lys Leu Ala Leu Val Ala Xaa Xaa 1 5 10 15 Val Ala Ala Met Val Ala Gly Arg Val Val Ala Ile Gly Asp Lys Pro 20 25 30 Gly Pro Asn Ile Thr Ala Thr Tyr Gly Xaa Lys Trp Leu Glu Ala Lys 35 40 45 Ala Thr Phe Tyr Gly Ser Asn Pro Arg Gly Ala Ala Pro Asp Asp His 50 55 60 Gly Gly Ala Cys Gly Tyr Xaa Xaa Val Asp Lys Pro Pro Phe Asp Gly 65 70 75 80 Met Thr Ala Cys Gly Asn Glu Pro Ile Phe Lys Asp Gly Leu Gly Cys 85 90 95 Gly Ala Cys Tyr Glu Ile Lys Cys Lys Glu Pro Val Glu Cys Ser Gly 100 105 110 Glu Pro Val Leu Val Lys Ile Thr Asp Lys Asn Tyr Glu His Ile Ala 115 120 125 Ala Tyr His Phe Asp Leu Ser Gly Lys Ala Phe Gly Ala Met Ala Lys 130 135 140 Lys Gly Gln Glu Asp Lys Leu Arg Lys Ala Gly Glu Leu Thr Leu Gln 145 150 155 160 Phe Arg Arg Val Lys Cys Lys Tyr Pro Ser Gly Thr Lys Ile Thr Phe 165 170 175 His Ile Glu Lys Gly Ser Asn Asp His Tyr Leu Ala Leu Leu Val Lys 180 185 190 Tyr Ala Ala Gly Asp Gly Asn Ile Val Ala Val Asp Ile Lys Pro Lys 195 200 205 Asp Ser Asp Glu Phe Ile Pro Met Lys Ser Ser Trp Gly Ala Ile Trp 210 215 220 Arg Ile Asp Pro Lys Lys Pro Leu Lys Gly Pro Phe Ser Ile Arg Leu 225 230 235 240 Thr Ser Glu Gly Gly Ala His Leu Val Gln Asp Asp Val Ile Pro Ala 245 250 255 Asn Trp Lys Pro Asp Thr Val Tyr Thr Ser Lys Leu Gln Phe Gly Ala 260 265 270 145 amino acids amino acid linear peptide internal Modified-site 58 /note= “Xaa is an unknown amino acid” Modified-site 77 /note= “Xaa is an unknown amino acid” Modified-site 87 /note= “Xaa is an unknown amino acid” Modified-site 126 /note= “Xaa is an unknown amino acid” 16 His Ile Ala Ala Tyr His Phe Asp Leu Ser Gly Lys Ala Phe Gly Ala 1 5 10 15 Met Ala Lys Lys Gly Glu Glu Asp Lys Leu Arg Lys Ala Gly Glu Leu 20 25 30 Met Leu Gln Phe Arg Arg Val Lys Cys Glu Tyr Pro Ser Asp Thr Lys 35 40 45 Ile Ala Phe His Val Glu Lys Gly Ser Xaa Pro Asn Tyr Leu Ala Leu 50 55 60 Leu Val Lys Tyr Ala Ala Gly Asp Gly Asn Ile Val Xaa Val Asp Ile 65 70 75 80 Lys Xaa Lys Gly Ser Asp Xaa Phe Leu Pro Met Lys Gln Ser Trp Gly 85 90 95 Ala Ile Trp Arg Ile Asp Pro Pro Lys Pro Leu Lys Gly Pro Phe Thr 100 105 110 Ile Arg Leu Thr Ser Glu Ser Gly Gly His Val Glu Gln Xaa Asp Val 115 120 125 Ile Pro Glu Asp Trp Lys Pro Asp Thr Val Tyr Lys Ser Lys Ile Gln 130 135 140 Phe 145 594 base pairs nucleic acid single linear cDNA 17 GACCTTTCTG GCAAGGCGTT CGGCGCCATG GCCAAGAAGG GCGAGGAGGA CAAGCTGCGC 60 AAGGCCGGCG AGCTGATGCT GCAGTTCCGC CGCGTCAAGT GCGAGTACCC ATCCGACACC 120 AAGATCGCCT TCCACGTTGA GAAGGGCTCC AACCCCAATT ACCTGGCGCT GCTCGTGAAG 180 TACGCGGCCG GCGACGGCAA TATCGTCAGT GTCGATATCA AGTCCAAGGG CTCCGACGAC 240 TTCCTGCCCA TGAAGCAGTC GTGGGGCGCC ATCTGGAGGA TCGATCCCCC CAAGCCGCTC 300 AAGGGTCCCT TCACGATCCG CCTCACCAGC GAGAGTGGCG GCCATGTCGA ACAGGAAGAT 360 GTCATCCCCG AAGACTGGAA GCCCGACACC GTCTACAAGT CCAAGATCCA GTTCTGAGCC 420 TGATGTGCCC ACAAACAGCG TGCACACTAA TAACACAACC TTATGACATC TTTGTTTCTT 480 TTTTGCAAGA AACAGTCTAT GCGATCTGCA TGCATGCATA CATATAATAA CAAGTATCGA 540 TGCGCGCGTG AGGTTTTTCT CTCCTTTTCT TTCTACTATT ATTGTTGCAT TTCC 594 802 base pairs nucleic acid single linear cDNA 18 GACAAGCCTC CCTTCGACGG CATGACCGCC TGCGGCAACG AGCCCATCTT CAAGGACGGC 60 CTCGGCTGCG GCGCATGCTA CGAGATCAAG TGCAAGGAAC CCGTCGAGTG CTCCGGCGAG 120 CCCGTCCTCG TCAAGATCAC CGACAAGAAC TACGAGCACA TCGCCGCCTA CCACTTCGAC 180 CTCTCCGGCA AGGCCTTCGG CGCCATGGCC AAGAAGGGCC AGGAAGACAA GCTGCGCAAG 240 GCCGGTGAGC TGACTCTGCA GTTCCGCCGC GTCAAGTGCA AGTACCCCTC CGGCACCAAG 300 ATCACCTTCC ACATCGAGAA GGGATCCAAC GACCATTACC TGGCGCTGCT CGTCAAGTAC 360 GCGGCCGGCG ATGGCAACAT TGTTGCTGTC GACATCAAGC CCAAGGACTC CGACGAGTTC 420 ATTCCCATGA AGTCGTCCTG GGGCGCCATC TGGAGGATCG ACCCCAAGAA GCCGCTCAAG 480 GGCCCCTTCT CCATCCGCCT CACCTCCGAG GGCGGCGCCC ATCTCGTCCA AGACGACGTC 540 ATCCCAGCCA ACTGGAAGCC AGACACCGTC TACACCTCCA AGCTCCAGTT CTAAACACGC 600 AAAGGCTTAT ATTTGGAGCA TATGAAGAAT GCACACAAGC ATGTGCTTCA GCTTCTCTTT 660 TCTTTACTTT CCTTCATTGC ATTGCATCTC ATCATCTCCA TATGTTTTTT AGATTTTGTG 720 ATGCAAAGTG TCATAAGTGC CAAGGATTCA GGAGGCGCTT TAAGCAGTGT CGAGGATGTA 780 GGGATCTCGT GCCGCTCGTG CC 802 832 base pairs nucleic acid single linear cDNA 19 CGACAAGCCT CCCTTCGACG GCATGACCGC CTGCGGCAAC GAGCCCATCT TCAAGGACGG 60 CCTCGGCTGC GGCGCATGCT ACGAGATCAA GTGCAAGGAA CCCGTCGAGT GCTCCGGCGA 120 GCCCGTCCTC GTCAAGATCA CCGACAAGAA CTACGAGCAC ATCGCCGCCT ACCACTTCGA 180 CCTCTCCGGC AAGGCCTTCG GCGCCATGGC CAAGAAGGGC CAGGAAGACA AGCTGCGCAA 240 GGCCGGTGAG CTGACTCTGC AGTTCCGCCG CGTCAAGTGC AAGTACCCCT CCGGCACCAA 300 GATCACCTTC CACATCGAGA AGGGATCCAA CGACCATTAC CTGGCGCTGC TCGTCAAGTA 360 CGCCGCCGGC GATGGCAACA TTGTCGCCGT CGACATCAAG CCCAAGGACT CCGACGAGTT 420 CATTCCCATG AAGTCGTCCT GGGGCGCCAT CTGGAGGATC GACCCCAAGA AGCCGCTCAA 480 GGGCCCCTTC TCCATCCGCC TCACCTCCGA GGGCGGCGCC CATCTCGTCC AGGACGACGT 540 CATCCCAGCC AACTGGAAGC CAGACACCGT CTACACCTCC AAGCTCCAGT TCTAAACACG 600 CAAAGGCTTA TATTTGGAGC ATATGAAGAA TGCTCTCAAG CATGTGCTTC AGGAGTGCCC 660 ACGATGTAGG GATAACCGAT TCATCAAAGC ACATCATGTG AAACATCAGT TGAAAAAACT 720 GGTTGATTTT TTTATTATTA TCGTGTAGAT TTGGATGCTT TTGAAATCTT TTGTATTCTT 780 CATTGAGTTT ACAAAATTAC GCAATTGATG AGAGATGCCC TCTTGCATTT TT 832 759 base pairs nucleic acid single linear cDNA CDS 1..738 CDS 742..759 20 GCC ATC GGC GAC AAG CCA GGG CCC AAC ATC ACG GCG ACC TAC GGC AGC 48 Ala Ile Gly Asp Lys Pro Gly Pro Asn Ile Thr Ala Thr Tyr Gly Ser 1 5 10 15 AAG TGG CTG GAG GCC AGG GCC ACC TTC TAC GGC AGC AAC CCG CGC GGT 96 Lys Trp Leu Glu Ala Arg Ala Thr Phe Tyr Gly Ser Asn Pro Arg Gly 20 25 30 GCC GCC CCC GAT GAC CAC GGC GGC GCT TGC GGG TAC AAG GAC GTC GAC 144 Ala Ala Pro Asp Asp His Gly Gly Ala Cys Gly Tyr Lys Asp Val Asp 35 40 45 AAG CCT CCC TTC GAC GGC ATG ACC GCC TGC GGC AAC GAG CCC ATC TTC 192 Lys Pro Pro Phe Asp Gly Met Thr Ala Cys Gly Asn Glu Pro Ile Phe 50 55 60 AAG GAC GGC CTC GGC TGC GGC GCA TGC TAC GAG ATC AAG TGC AAG GAA 240 Lys Asp Gly Leu Gly Cys Gly Ala Cys Tyr Glu Ile Lys Cys Lys Glu 65 70 75 80 CCC GTC GAG TGC TCC GGC GAG CCC GTC CTC GTC AAG ATC ACC GAC AAG 288 Pro Val Glu Cys Ser Gly Glu Pro Val Leu Val Lys Ile Thr Asp Lys 85 90 95 AAC TAC GAG CAC ATC GCC GCC TAC CAC TTC GAC CTC TCC GGC AAG GCC 336 Asn Tyr Glu His Ile Ala Ala Tyr His Phe Asp Leu Ser Gly Lys Ala 100 105 110 TTC GGC GCC ATG GCC AAG AAG GGC CAG GAA GAC AAG CTG CGC AAG GCC 384 Phe Gly Ala Met Ala Lys Lys Gly Gln Glu Asp Lys Leu Arg Lys Ala 115 120 125 GGT GAG CTG ACT CTG CAG TTC CGC CGC GTC AAG TGC AAG TAC CCC TCC 432 Gly Glu Leu Thr Leu Gln Phe Arg Arg Val Lys Cys Lys Tyr Pro Ser 130 135 140 GGC ACC AAG ATC ACC TTC CAC ATC GAG AAG GGA TCC AAC GAC CAT TAC 480 Gly Thr Lys Ile Thr Phe His Ile Glu Lys Gly Ser Asn Asp His Tyr 145 150 155 160 CTG GCG CTG CTC GTC AAG TAC GCG GCC GGC GAT GGC AAC ATT GTC GCC 528 Leu Ala Leu Leu Val Lys Tyr Ala Ala Gly Asp Gly Asn Ile Val Ala 165 170 175 GTC GAC ATC AAG CCC AGG GAC TCC GAC GAG TTC ATT CCC ATG AAG TCG 576 Val Asp Ile Lys Pro Arg Asp Ser Asp Glu Phe Ile Pro Met Lys Ser 180 185 190 TCC TGG GGC GCC ATC TGG AGG ATC GAC CCC AAG AAG CCG CTC AAG GGC 624 Ser Trp Gly Ala Ile Trp Arg Ile Asp Pro Lys Lys Pro Leu Lys Gly 195 200 205 CCC TTC TCC ATC CGC CTC ACC TCC GAG GGC GGC GCC CAT CTC GTC CAG 672 Pro Phe Ser Ile Arg Leu Thr Ser Glu Gly Gly Ala His Leu Val Gln 210 215 220 GAC GAC GTC ATC CCA GCC AAC TGG AAG CCA GAC ACC GTC TAC ACC TCC 720 Asp Asp Val Ile Pro Ala Asn Trp Lys Pro Asp Thr Val Tyr Thr Ser 225 230 235 240 AAG CTC CAG TTC GGA GCC TGA GAG ACG ATG ATC CTC CAT 759 Lys Leu Gln Phe Gly Ala * 245 246 amino acids amino acid linear protein 21 Ala Ile Gly Asp Lys Pro Gly Pro Asn Ile Thr Ala Thr Tyr Gly Ser 1 5 10 15 Lys Trp Leu Glu Ala Arg Ala Thr Phe Tyr Gly Ser Asn Pro Arg Gly 20 25 30 Ala Ala Pro Asp Asp His Gly Gly Ala Cys Gly Tyr Lys Asp Val Asp 35 40 45 Lys Pro Pro Phe Asp Gly Met Thr Ala Cys Gly Asn Glu Pro Ile Phe 50 55 60 Lys Asp Gly Leu Gly Cys Gly Ala Cys Tyr Glu Ile Lys Cys Lys Glu 65 70 75 80 Pro Val Glu Cys Ser Gly Glu Pro Val Leu Val Lys Ile Thr Asp Lys 85 90 95 Asn Tyr Glu His Ile Ala Ala Tyr His Phe Asp Leu Ser Gly Lys Ala 100 105 110 Phe Gly Ala Met Ala Lys Lys Gly Gln Glu Asp Lys Leu Arg Lys Ala 115 120 125 Gly Glu Leu Thr Leu Gln Phe Arg Arg Val Lys Cys Lys Tyr Pro Ser 130 135 140 Gly Thr Lys Ile Thr Phe His Ile Glu Lys Gly Ser Asn Asp His Tyr 145 150 155 160 Leu Ala Leu Leu Val Lys Tyr Ala Ala Gly Asp Gly Asn Ile Val Ala 165 170 175 Val Asp Ile Lys Pro Arg Asp Ser Asp Glu Phe Ile Pro Met Lys Ser 180 185 190 Ser Trp Gly Ala Ile Trp Arg Ile Asp Pro Lys Lys Pro Leu Lys Gly 195 200 205 Pro Phe Ser Ile Arg Leu Thr Ser Glu Gly Gly Ala His Leu Val Gln 210 215 220 Asp Asp Val Ile Pro Ala Asn Trp Lys Pro Asp Thr Val Tyr Thr Ser 225 230 235 240 Lys Leu Gln Phe Gly Ala 245 368 base pairs nucleic acid single linear cDNA CDS 3..368 22 CC AAC ATC ACT GCA ACC TAC GGT GAC AAG TGG CTG GAT GCG AAG GCC 47 Asn Ile Thr Ala Thr Tyr Gly Asp Lys Trp Leu Asp Ala Lys Ala 1 5 10 15 ACG TTC TAC GGC AGC GAC CCA CGT GGC GCG GCC CCC GAT GAC CAT GGC 95 Thr Phe Tyr Gly Ser Asp Pro Arg Gly Ala Ala Pro Asp Asp His Gly 20 25 30 GGC GCG TGC GGA TAC AAG GAC GTC GAC AAG GCA CCC TTC GAC AGC ATG 143 Gly Ala Cys Gly Tyr Lys Asp Val Asp Lys Ala Pro Phe Asp Ser Met 35 40 45 ACT GGA TGC GGC AAC GAG CCC ATC TTC AAG GAC GGT CTG GGC TGC GGC 191 Thr Gly Cys Gly Asn Glu Pro Ile Phe Lys Asp Gly Leu Gly Cys Gly 50 55 60 TCC TGC TAC GAG ATC AAG TGC AAG GAG CCA GCC GAG TGC TCA GGC GAG 239 Ser Cys Tyr Glu Ile Lys Cys Lys Glu Pro Ala Glu Cys Ser Gly Glu 65 70 75 CCC GTC CTC ATT AAG ATC ACC GAC AAG AAC TAC GAG CAC ATC GCC GCC 287 Pro Val Leu Ile Lys Ile Thr Asp Lys Asn Tyr Glu His Ile Ala Ala 80 85 90 95 TAC CAC TTC GAC CTT TCT GGC AAG GCG TTC GGC GCC ATG GCC AAG AAG 335 Tyr His Phe Asp Leu Ser Gly Lys Ala Phe Gly Ala Met Ala Lys Lys 100 105 110 GGC GAG GAG GAC AAG CTG CGC AAG GCC GGC GAG 368 Gly Glu Glu Asp Lys Leu Arg Lys Ala Gly Glu 115 120 122 amino acids amino acid linear protein 23 Asn Ile Thr Ala Thr Tyr Gly Asp Lys Trp Leu Asp Ala Lys Ala Thr 1 5 10 15 Phe Tyr Gly Ser Asp Pro Arg Gly Ala Ala Pro Asp Asp His Gly Gly 20 25 30 Ala Cys Gly Tyr Lys Asp Val Asp Lys Ala Pro Phe Asp Ser Met Thr 35 40 45 Gly Cys Gly Asn Glu Pro Ile Phe Lys Asp Gly Leu Gly Cys Gly Ser 50 55 60 Cys Tyr Glu Ile Lys Cys Lys Glu Pro Ala Glu Cys Ser Gly Glu Pro 65 70 75 80 Val Leu Ile Lys Ile Thr Asp Lys Asn Tyr Glu His Ile Ala Ala Tyr 85 90 95 His Phe Asp Leu Ser Gly Lys Ala Phe Gly Ala Met Ala Lys Lys Gly 100 105 110 Glu Glu Asp Lys Leu Arg Lys Ala Gly Glu 115 120 245 amino acids amino acid linear peptide internal Modified-site 157 /note= “Xaa is Ser or Asn” Modified-site 176 /note= “Xaa is Gly or Ser” Modified-site 181 /note= “Xaa is Pro or Ser” Modified-site 187 /note= “Xaa is Glu or Asp” Modified-site 226 /note= “Xaa is Asp or Glu” 24 Val Ala Ile Xaa Asp Lys Pro Gly Pro Asn Ile Thr Ala Thr Tyr Gly 1 5 10 15 Asp Lys Trp Leu Asp Ala Lys Ala Thr Phe Tyr Gly Ser Asp Pro Arg 20 25 30 Gly Ala Ala Pro Asp Asp His Gly Gly Ala Cys Gly Tyr Lys Asp Val 35 40 45 Asp Lys Ala Pro Phe Asp Ser Met Thr Gly Cys Gly Asn Glu Pro Ile 50 55 60 Phe Lys Asp Gly Leu Gly Cys Gly Ser Cys Tyr Glu Ile Lys Cys Lys 65 70 75 80 Glu Pro Ala Glu Cys Ser Gly Glu Pro Val Leu Ile Lys Ile Thr Asp 85 90 95 Lys Asn Tyr Glu His Ile Ala Ala Tyr His Phe Asp Leu Ser Gly Lys 100 105 110 Ala Phe Gly Ala Met Ala Lys Lys Gly Glu Glu Asp Lys Leu Arg Lys 115 120 125 Ala Gly Glu Leu Met Leu Gln Phe Arg Arg Val Lys Cys Glu Tyr Pro 130 135 140 Ser Asp Thr Lys Ile Ala Phe His Val Glu Lys Gly Ser Xaa Pro Asn 145 150 155 160 Tyr Leu Ala Leu Leu Val Lys Tyr Ala Ala Gly Asp Gly Asn Ile Val 165 170 175 Xaa Val Asp Ile Lys Xaa Lys Gly Ser Asp Xaa Phe Leu Pro Met Lys 180 185 190 Gln Ser Trp Gly Ala Ile Trp Arg Ile Asp Pro Pro Lys Pro Leu Lys 195 200 205 Gly Pro Phe Thr Ile Arg Leu Thr Ser Glu Ser Gly Gly His Val Glu 210 215 220 Gln Xaa Asp Val Ile Pro Glu Asp Trp Lys Pro Asp Thr Val Tyr Lys 225 230 235 240 Ser Lys Ile Gln Phe 245 26 amino acids amino acid linear peptide internal Modified-site /note= “Xaa is an unknown amino acid” Modified-site 18 /note= “Xaa is an unknown amino acid” 25 Ala Met Gly Asp Lys Pro Gly Pro Xaa Ile Thr Ala Thr Tyr Gly Asp 1 5 10 15 Lys Xaa Leu Asp Ala Lys Thr Ala Phe Asp 20 25 21 amino acids amino acid linear peptide internal Modified-site /note= “Xaa is an unknown amino acid” Modified-site 16 /note= “Xaa is an unknown amino acid” Modified-site 20 /note= “Xaa is an unknown amino acid” 26 Ala Ile Gly Asp Lys Pro Gly Pro Xaa Ile Thr Ala Trp Tyr Gly Xaa 1 5 10 15 Lys Thr Leu Xaa Ala 20 34 amino acids amino acid linear peptide internal Modified-site /note= “Xaa is an unknown amino acid” Modified-site 15-16 /note= “Xaa is an unknown amino acid” 27 Ala Ile Gly Asp Lys Pro Gly Pro Xaa Ile Thr Ala Thr Tyr Xaa Xaa 1 5 10 15 Lys Trp Leu Asp Ala Lys Ala Thr Phe Tyr Gly Ser Asn Pro Arg Gly 20 25 30 Ala Ala 30 base pairs nucleic acid single linear cDNA 28 GGGTCTAGAG GTACCGTCCG ATCGATCATT 30 13 base pairs nucleic acid single linear cDNA 29 AATGATCGAT GCT 13 20 base pairs nucleic acid single linear cDNA 30 GGGTCTAGAG GTACCGTCCG 20 18 base pairs nucleic acid single linear cDNA 31 GATGTGCTCG TAGTTCTT 18 6 amino acids amino acid linear peptide internal 32 Lys Asn Tyr Glu His Ile 1 5 24 base pairs nucleic acid single linear cDNA 33 GGGGATCCGA GGCCGTCCTT GAAG 24 6 amino acids amino acid linear peptide internal 34 Ile Phe Lys Asp Gly Leu 1 5 26 amino acids amino acid linear peptide internal 35 Ala Ile Gly Asp Lys Pro Gly Pro Asn Ile Thr Ala Thr Gly Asn Lys 1 5 10 15 Trp Leu Glu Ala Lys Ala Thr Phe Tyr Gly 20 25 26 amino acids amino acid linear peptide internal 36 Ala Ile Gly Asp Lys Pro Gly Pro Asn Ile Thr Ala Thr Gly Ser Lys 1 5 10 15 Trp Leu Glu Ala Lys Ala Thr Phe Tyr Gly 20 25 27 base pairs nucleic acid single linear cDNA 37 GGGAATTCGC CATCGGCGAC AAGCCAG 27 26 base pairs nucleic acid single linear cDNA 38 CCCTGCAGAT GGAGGATCAT CGTCTC 26 32 base pairs nucleic acid single linear cDNA 39 TTTCTAGAGC CATCGGCGAC AAGCCAGGGC CC 32 29 base pairs nucleic acid single linear cDNA 40 GCGTACTTCA CGAGCAGCGC CAGGTAATT 29 27 amino acids amino acid linear peptide internal Modified-site /note= “Xaa is an unknown amino acid” 41 Ala Met Gly Asp Lys Pro Gly Pro Xaa Ile Thr Ala Thr Tyr Gly Asp 1 5 10 15 Lys Trp Leu Asp Ala Lys Ala Thr Phe Tyr Gly 20 25 26 amino acids amino acid linear peptide internal Modified-site /note= “Xaa is an unknown amino acid” Modified-site 18 /note= “Xaa is an unknown amino acid” 42 Ala Ile Gly Asp Lys Pro Gly Pro Xaa Ile Thr Ala Thr Tyr Gly Ser 1 5 10 15 Lys Xaa Leu Glu Ala Lys Ala Thr Phe Tyr 20 25 14 amino acids amino acid linear peptide internal Modified-site /note= “Xaa is an unknown amino acid” 43 Ala Met Gly Asp Lys Pro Gly Pro Xaa Ile Thr Ala Val Tyr 1 5 10 30 amino acids amino acid linear peptide internal Modified-site /note= “Xaa is an unknown amino acid” 44 Ile Ala Lys Val Pro Pro Gly Pro Asn Ile Thr Ala Glu Tyr Gly Asp 1 5 10 15 Lys Trp Leu Asp Ala Lys Ser Thr Trp Tyr Gly Lys Pro Thr 20 25 30 24 amino acids amino acid linear peptide internal Modified-site 15-16 /note= “Xaa is an unknown amino acid” 45 Ala Ile Gly Asp Lys Pro Gly Pro Lys Ile Thr Ala Thr Tyr Xaa Xaa 1 5 10 15 Lys Trp Leu Glu Ala Lys Ala Thr 20 

What is claimed is:
 1. An isolated nucleic acid sequence coding for a Bermuda grass pollen protein allergen, Cyn dI, wherein the Cyn dI protein allergen comprises an amino acid sequence selected from the group consisting of Cyn dI.18 (SEQ ID No: 15), Cyn dI.CD1 (SEQ ID NO: 21) and Cyn dI2/3 (SEQ ID NO: 24), all as shown in FIG.
 20. 2. An isolated nucleic acid sequence coding for a Bermuda grass pollen protein allergen Cyn dI, having the formula: L₁NYX wherein L1 is a nucleic acid sequence of 0-300 nucleotides which nucleic acid sequence includes nucleotides encoding a leader sequence of Cyn dI, N is a nucleic acid sequence comprising up to 600 nucleotides which nucleic acid sequence contains nucleotides encoding the amino terminus portion of mature Cyn dI, Y is the portion of the nucleic acid sequence of clone 2 (SEQ ID NO: 1), clone 18 (SEQ ID NO: 3), clone 3 (SEQ ID NO: 17), clone 22 (SEQ ID NO: 18), clone 23 (SEQ ID NO: 19) or any polymorphic form thereof that codes for mature Cyn dI, and X is a nucleic acid sequence of 0-600 nucleotides which nucleic acid sequence contains nucleotides of the 3′ untranslated portion of Cyn dI, and wherein L₁ and X can be
 0. 3. An isolated nucleic acid sequence of claim 2 having the formula: L₁NYX wherein L₁ is a nucleic acid sequence of 0-300 nucleotides which nucleic acid sequence includes nucleotides encoding a leader sequence of Cyn dI, N is a nucleic acid sequence comprising up to 600 nucleotides which nucleic acid sequence contains nucleotides encoding the amino terminus portion of mature Cyn dI, Y is the portion of the nucleic acid sequence of clone 2, clone 18, clone 3, clone 22, clone 23, or any polymorphic form thereof that codes for mature Cyn dI, and X is a nucleic acid sequence of 0-600 nucleotides which nucleic acid sequence includes nucleotides of the 3′ untranslated portion of Cyn dI, and wherein the nucleic acid sequence of N does not overlap the 5′ end of the nucleic acid sequence of Y and wherein L₁ and X can be
 0. 4. An isolated nucleic acid sequence of claim 3, wherein L₁ is the nucleic acid sequence represented by nucleotides 1-106 of clone 14a1 (SEQ ID NO: 10) as shown if FIG. 6, or nucleotides 1-103 of clone 14c1 (SEQ ID NO: 12) as shown in FIG
 7. 5. An isolated nucleic acid sequence of claim 4, wherein N is the nucleic acid sequence represented by nucleotides 107-244 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6 or the nucleic acid sequence represented by nucleotides 104-243 of clone 14c1 (SEQ ID NO: 12) as shown in FIG. 7, Y is the nucleic acid sequence represented by nucleotides 1-603 of clone 18 (SEQ ID NO: 3) as shown in FIG. 2 and the nucleic acid sequence of X contains nucleotides 604-775 of clone 18 (SEQ ID NO: 3) as shown in FIG.
 2. 6. An isolated nucleic acid sequence of claim 4, wherein N is the nucleic acid sequence represented by nucleotides 107-244 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6 or the nucleic aced sequence represented by nucleotides 104-246 of clone 14c1 (SEQ ID NO: 12) as shown in FIG. 7, Y is the nucleic acid sequence represented by nucleotides 1-594 of clone 22 (SEQ ID NO: 18) as shown in FIG. 16, and the nucleic acid sequence of X contains nucleotides 595-802 of clone 22 (SEQ ID NO: 18) as shown in FIG.
 16. 7. An isolated nucleic acid sequence of claim 4, wherein N is the nucleic acid sequence represented by nucleotides 107-246 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6 or the nucleic acid sequence represented by nucleotides 104-245 of clone 14c1 (SEQ ID NO: 12) as shown in FIG. 7, Y is the nucleic acid sequence represented by nucleotides 1-595 of clone 23 (SEQ ID NO: 19) as shown in FIG. 17, and the nucleic acid sequence of X contains nucleotides 596-832 of clone 23 (SEQ ID NO: 19) as shown in FIG. 17).
 8. An isolated nucleic acid sequence of claim 3, wherein L₁ comprised the nucleic acid sequence represented by nucleotides 41-106 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6, or nucleotides 28-103 of clone 14c1 (SEQ ID NO: 12) as shown in FIG.
 7. 9. An isolated nucleic acid sequence of claim 8, wherein N is the nucleic acid sequence represented by nucleotides 107-244 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6 or the nucleic acid sequence represented by nucleotides 104-243 of clone 14c1 (SEQ ID NO: 12) as shown if FIG. 7, Y is the nucleic acid sequence represented by nucleotides 1-603 of clone 18 (SEQ ID NO: 3) as shown in FIG. 2 and X is
 0. 10. An isolated nucleic acid sequence of claim 8, wherein N is the nucleic acid sequence represented by nucleotides 107-247 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6 or the nucleic acid sequence represented by nucleotides 104-246 of clone 14c1 (SEQ ID NO: 12) as shown in FIG. 7, Y is the nucleic acid sequence represented by nucleotides 1-594 of clone 22 (SEQ ID NO: 18) as shown in FIG. 16, and X is
 0. 11. An isolated nucleic acid sequence of claim 8, wherein N is the nucleic acid sequence represented by nucleotides 107-246 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6 or the nucleic acid sequence represented by nucleotides 104-245 of clone 14c1 (SEQ ID NO: 12) as shown in FIG. 7, Y is the nucleic acid sequence represented by nucleotides 1-595 of clone 23 (SEQ ID NO: 19) as shown in FIG. 17, and X is
 0. 12. An isolated nucleic acid sequence of claim 3, wherein L₁ is 0, N is the nucleic acid sequence represented by nucleotides 107-244 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6 or the nucleic acid sequence represented by nucleotides 104-243 of clone 14c1 (SEQ ID NO: 12) as shown in FIG. 7, Y is the nucleic acid sequence represented by nucleotides 1-603 of clone 18 (SEQ ID NO: 3) as shown in FIG. 2 and X is
 0. 13. An isolated nucleic acid sequence of claim 3, wherein L₁ is 0, N is the nucleic acid sequence represented by nucleotides 107-247 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6 or the nucleic acid sequence represented by nucleotides 104-246 of clone 14c1 (SEQ ID NO: 12) as shown in FIG. 7, Y is the nucleic acid sequence represented by nucleotides 1-594 of clone 22 (SEQ ID NO: 18) as shown in FIG. 16, and X is
 0. 14. An isolated nucleic acid sequence of claim 3, wherein L₁ is 0, N is the nucleic acid sequence represented by nucleotides 107-246 of clone 14a1 (SEQ ID NO: 10) as shown in FIG. 6 or the nucleic acid sequence represented by nucleotides 104-245 of clone 14c1 (SEQ ID NO: 12) as shown in FIG. 7, Y is the nucleic acid sequence represented by nucleotides 1-595 of clone 23 (SEQ ID NO: 19) as shown in FIG. 17, and X is
 0. 15. An isolated nucleic acid sequence of claim 3, wherein Y is a nucleic acid sequence represented by nucleotides 1-438 of clone 2 (SEQ ID NO: 1) as shown in FIG.
 1. 16. An isolated nucleic acid sequence of claim 3, wherein Y is a nucleic acid sequence represented by nucleotides 1-417 of clone 3 (SEQ ID NO: 17) as shown in FIG. 15 and X is a nucleic acid sequence represented by nucleotides 418-594 of clone 3 (SEQ ID NO: 17) as shown in FIG.
 15. 17. An isolated nucleic acid sequence of claim 3, wherein L₁ is 0, Y is a nucleic acid sequence represented by nucleotides 1-438 of clone 2 (SEQ ID NO: 1) as shown in FIG. 1 and X is
 0. 18. An isolated nucleic acid sequence of claim 3, wherein L₁ is 0, Y is a nucleic acid sequence represented by nucleotides 1-417 of clone 3 (SEQ ID NO: 17) as shown in FIG. 15 and X is
 0. 19. An isolated nucleic acid sequence coding for a Bermuda grass pollen protein allergen, Cyn dI, wherein the Cyn dI allergen is encoded by the nucleic acid sequence of clone CD1 as shown in FIG. 18 (SEQ ID NO: 20), or a portion thereof encoding at least one T cell epitope of Cyn dI.
 20. An isolated nucleic acid sequence coding for a Bermuda grass pollen allergen, Cyn dI, wherein the Cyn dI allergen comprises the amino acid sequence of Cyn dI.2/3 (full-length) as shown in FIG. 20 (SEQ ID NO: 24), or a portion thereof encoding at least one T cell epitope of Cyn dI.
 21. An expression vector comprising the nucleic acid sequence of claim
 1. 22. An expression vector comprising the nucleic acid sequence of claim
 3. 23. An expression vector comprising the nucleic acid sequence of claim
 19. 24. An expression vector comprising the nucleic acid sequence of claim
 20. 25. An expression vector comprising the nucleic acid sequence of claim
 2. 26. A host cell transformed to express a protein or peptide encoded by the nucleic acid sequence of claim
 1. 27. A host cell transformed to express a protein or peptide encoded by the nucleic acid sequence of claim
 3. 28. A host cell transformed to express a protein or a peptide comprising the nucleic acid sequence of claim
 19. 29. A host cell transformed to express a protein or a peptide comprising the nucleic acid sequence of claim
 20. 30. A host cell transformed to express a protein or a peptide comprising the nucleic acid sequence of claim
 12. 31. An isolated nucleic acid sequence as in any of claim 1, 2, 19 or 20, wherein said protein allergen is not a protein allergen of the species Lolium perenne, Lol pI. 